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						<title>CHPA Career Center Search Results (&#39;assistant OR profess OR STATECODE:&quot;SC&quot;&#39; Jobs)</title>
						<link>https://careers.chpa.org</link>
						<description>Latest CHPA Career Center Jobs</description>
						<pubDate>Fri, 24 Apr 2026 08:15:23 Z</pubDate>
						
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									<link>https://careers.chpa.org/jobs/rss/22186203/chief-executive-officer-the-manor</link>
								
								<title>Chief Executive Officer, The Manor | Deffet Group, Inc.</title>								
								<guid isPermaLink="true">https://careers.chpa.org/jobs/rss/22186203/chief-executive-officer-the-manor</guid>
								<description>Florence, South Carolina,  Deffet Group, Inc. is pleased to have been retained by  The Manor  to conduct an executive search for a  Chief Executive Officer . 
 The Manor (United Methodist Manor of the Pee Dee) is a vibrant, faith-based, not-for-profit Life Plan Community (LPC) located on a beautiful, 87-acre campus in Florence, South Carolina. Founded in 1982, the organization operates as a 501(c)(3) and serves older adults throughout the Pee Dee region. Steeped in traditional Southern values of service, hospitality, community and friendship, and care, The Manor is dedicated to providing residents with the highest quality housing, health care, services and amenities to support an independent, worry-free retirement. 
 The Manor is seeking a Chief Executive Officer (CEO) to lead the community in meeting the needs of the next generation. Reporting to the Board of Trustees, this individual will be a hands-on, articulate leader with a deep passion for senior living and proven ability in developing and implementing strategic plans. 
 The successful candidate for this position will have a Bachelor&#8217;s degree (Master&#8217;s highly preferred) and, ideally, a minimum of ten years&#8217; senior management experience in continuing care senior living facilities. Our finalist will excel at building positive and professional relationships with residents, team and board members, will have experience in financial management and budget processes, and will demonstrate in-depth knowledge of regulatory requirements and best practices in senior living operations. 
 This is an outstanding leadership opportunity for an individual who wants to lead a forward-looking community and to continue to build upon the organization&#8217;s outstanding reputation for providing an exceptional lifestyle rooted in hospitality and service. 
 Candidate nominations or expressions of personal interest may be directed in confidence to Dan Deffet, Managing Partner, Deffet Group, Inc., via email:  info@deffetgroup.com .</description>
								<pubDate>Wed, 08 Apr 2026 16:09:50 -0400</pubDate>
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									<link>https://careers.chpa.org/jobs/rss/22188899/clinical-dietitian-professional</link>
								
								<title>Clinical Dietitian Professional | Children&#39;s Hospital Colorado</title>								
								<guid isPermaLink="true">https://careers.chpa.org/jobs/rss/22188899/clinical-dietitian-professional</guid>
								<description>Aurora, Colorado,  Come be a part of our Clinical Nutrition Team! We are an incredible group of clinicians dedicated to providing patient &#38; family centered evidence-based medical nutrition therapy. Our clinical RDs are highly integrated within the multidisciplinary team on the inpatient units and outpatient clinics at Children&#8217;s Hospital Colorado. Come experience the culture of Clinical Nutrition&#8230;excellence, collaboration, partnership, and connection! 
 The Clinical Dietitian Professional is an experienced team member who provides comprehensive, safe, and ethical medical nutrition therapy to patients, families, and other clients in inpatient or outpatient settings.&#xa0; 
 Additional Information 
 
 Location/Department: &#xa0;Clinical Nutrition 
 Job Details: 1.0 FTE; 40 hours/week - eligible for benefits 
 Coverage and Schedule
 
 &#xa0;Weekday Coverage Primary inpatient and outpatient coverage at Anschutz Medical Campus within the Center for Cancer and Blood Disorders, including the Bone Marrow Transplant Unit, Hematology &#38; Oncology, and associated ambulatory clinics. Weekend Coverage: During scheduled weekend shifts, this role provides hospital wide Clinical Nutrition coverage, supporting patient needs beyond the primary weekday service areas. Schedule: Consistent weekend schedule for a minimum of 6 months. Thursday-Monday, 8:30 a.m.&#8211;5:00 p.m. 
 
 
 
 Duties &#38; Responsibilities 
 
 Assesses, plans, and delivers accurate medical nutrition therapy using established standards and evidence. 
 Collaborates as a member of committees, task forces, and/or workgroups. 
 Works collaboratively as a member of committees, task forces, and workgroups, and is involved in projects that support the organization&#8217;s mission. 
 Financial Responsibility: Assists in achieving departmental financial budget targets. 
 Incorporates principles of culture-competence and family-centered care. 
 Trains and observes RDs, interns, and students in their clinical practice. Provides feedback to enhance understanding and compliance. 
 Pursues professional growth and skill development. 
 Actively contributes to rounds, care conferences, and care coordination. Collaborates and promotes teamwork to achieve positive patient and client outcomes across the organization and/or within the department. 
 Proactively connects with Clinical Nutrition team members and other disciplines in the organization to identify Clinical Nutrition-related issues, potential solutions, and opportunities for quality and process improvement. 
 Ensures compliance with established regulatory standards and healthcare regulatory requirements by identifying and following policies and procedures for the nutritional care provided. 
 Accurately documents patient care and tracks time/activities for use with benchmarking, billing, and/or productivity in accordance with department standards. 
 Participates in advocacy, policy and procedure review, quality improvement and/or research. 
 
 Salary Information Pay is dependent on applicant&#39;s relevant experience. &#xa0;Pay ranges from &#xa0;$30.44 to&#xa0;$45.67/hour. These RD positions are eligible for the weekend differential during weekend shifts. 
 ***The stated range represents the full pay scale; however&#xa0; expected starting pay &#xa0;for this position is above the posted minimum of the range and will likely fall between $32.50 and $39.00/hour. 
 Effective June 2026, this position will transition from exempt to non exempt. As a non exempt role, team members will be eligible for overtime pay and may be eligible for applicable shift differentials in accordance with Children&#8217;s Hospital Colorado policy. Benefits Information Here, you matter. As a Children&#8217;s Hospital Colorado team member, you will receive a competitive pay and benefits package designed to take care of your needs that includes base pay, incentives, paid time off, medical/dental/vision insurance, company provided life and disability insurance, paid parental leave, 403b employer match (retirement savings), a robust wellness program, and access to professional development tools, including an education benefit to help you advance your career. 
 As part of our Total Rewards package, Children&#39;s Colorado offers an annual employee bonus program that rewards eligible team members based on organizational performance. If organizational goals are met for the year, the bonus is paid out the following April. 
 Children&#8217;s Colorado delivers annual base pay increases to eligible team members based on their performance over the previous year. Qualification Requirements 
 
 EDUCATION &#8211; &#xa0;Bachelor&#39;s Degree (prior to 2024 graduates). Master&#8217;s Degree required for 2024 (and beyond) graduates. 
 EXPERIENCE &#8211; &#xa0;Two (2) years clinical nutrition required. 
 LICENSURES &#8211; Registered Dietitians (RD) or Registered Dietitian Nutritionists (RDN) adhering to the Commission of Dietetic Registration guidelines. CNSC, CSO, or CSP preferred. &#xa0;</description>
								<pubDate>Thu, 09 Apr 2026 11:42:33 -0400</pubDate>
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									<link>https://careers.chpa.org/jobs/rss/22200202/clinical-dietitian</link>
								
								<title>Clinical Dietitian | Children&#39;s Hospital Colorado</title>								
								<guid isPermaLink="true">https://careers.chpa.org/jobs/rss/22200202/clinical-dietitian</guid>
								<description>Aurora, Colorado,  Come be a part of our Clinical Nutrition Team! We are an incredible group of clinicians dedicated to providing patient &#38; family centered evidence-based medical nutrition therapy. Our clinical RDs are highly integrated within the multidisciplinary team on the inpatient units and outpatient clinics at Children&#8217;s Hospital Colorado. Come experience the culture of Clinical Nutrition&#8230;excellence, collaboration, partnership, and connection! 
 The Clinical Dietitian Professional is an experienced team member who provides comprehensive, safe, and ethical medical nutrition therapy to patients, families, and other clients in inpatient or outpatient settings. &#xa0;This position will be a part of our dedicated General Medicine RD team, supporting a variety of patients, ages, and nutrition needs both on our hospital medicine teams, trauma acute care team, Rehab team with associated outpatient clinics and inpatient Orthopedics and High-Risk Spine Clinic. &#xa0;This is an excellent position for someone who is eager to learn, grown in their pediatric nutrition expertise, and become a part of a dynamic team.&#xa0; 
 Additional Information 
 
 Location/Dept: &#xa0;Clinical Nutrition 
 Job Information: 1.0 FTE; 40 hours/week - eligible for benefits 
 Shift: &#xa0;5x8&#39;s (M-F) with intermittent weekend/holiday coverage.&#xa0; &#xa0; 
 
 ESSENTIAL FUNCTIONS An employee in this position may be called upon to do any or all of the following essential functions. These examples do not include all of the functions which the employee may be expected to perform. 
 1.&#xa0;&#xa0;&#xa0;&#xa0;Assesses, plans, and delivers accurate medical nutrition therapy using established standards and evidence.&#xa0; 2.&#xa0;&#xa0;&#xa0;&#xa0;Incorporates principles of culture-competence and family-centered care. 3.&#xa0;&#xa0;&#xa0;&#xa0;Trains and observes RDs, interns, and students in their clinical practice. Provides feedback to enhance understanding and compliance. 4.&#xa0;&#xa0;&#xa0;&#xa0;Pursues professional growth and skill development.&#xa0; 5.&#xa0;&#xa0;&#xa0;&#xa0;Actively contributes to rounds, care conferences, and care coordination. Collaborates and promotes teamwork to achieve positive patient and client outcomes across the organization and/or within the department. 6.&#xa0;&#xa0;&#xa0;&#xa0;Proactively connects with Clinical Nutrition team members and other disciplines in the organization to identify Clinical Nutrition-related issues, potential solutions, and opportunities for quality and process improvement. 7.&#xa0;&#xa0;&#xa0;&#xa0;Ensures compliance with established regulatory standards and healthcare regulatory requirements by identifying and following policies and procedures for the nutritional care provided. 8.&#xa0;&#xa0;&#xa0;&#xa0;Accurately documents patient care and tracks time/activities for use with benchmarking, billing, and/or productivity in accordance with department standards.&#xa0; 9.&#xa0;&#xa0;&#xa0;&#xa0;Participates in advocacy, policy and procedure review, quality improvement and/or research. 10.&#xa0;&#xa0;&#xa0;&#xa0;Collaborates as a member of committees, task forces, and/or workgroups.&#xa0; 11.&#xa0;&#xa0;&#xa0;&#xa0;Works collaboratively as a member of committees, task forces, and workgroups, and is involved in projects that support the organization&#8217;s mission. 12.&#xa0;&#xa0;&#xa0;&#xa0;Financial Responsibility: Assists in achieving departmental financial budget targets.&#xa0; 
 Salary Information Pay is dependent on applicant&#39;s relevant experience. Annual Salary Range (Based on 40 hours worked per week): &#xa0;$63,317.59&#xa0;to&#xa0;$94,976.38 (Hourly rate of $30.44&#xa0;to&#xa0;$45.66). &#xa0;&#xa0;&#xa0; 
 ***The stated range represents the full pay scale; &#xa0;however expected starting pay for this position is above the posted minimum of the range &#xa0;and will likely fall between $32.50 &#8211; $39/hour or $67,600 - $81,120/year). 
 Benefits Information Here, you matter. As a Children&#8217;s Hospital Colorado team member, you will receive a competitive pay and benefits package designed to take care of your needs that includes base pay, incentives, paid time off, medical/dental/vision insurance, company provided life and disability insurance, paid parental leave, 403b employer match (retirement savings), a robust wellness program, and access to professional development tools, including an education benefit to help you advance your career. 
 As part of our Total Rewards package, Children&#39;s Colorado offers an annual employee bonus program that rewards eligible team members based on organizational performance. If organizational goals are met for the year, the bonus is paid out the following April. 
 Children&#8217;s Colorado delivers annual base pay increases to eligible team members based on their performance over the previous year. MINIMUM QUALIFICATIONS&#xa0; EDUCATION &#8211; &#xa0;Bachelor&#39;s Degree (prior to 2024 graduates). Master&#8217;s Degree required for 2024 (and beyond) graduates. EXPERIENCE &#8211; &#xa0;Two (2) years clinical nutrition LICENSURES &#8211; Registered Dietitians (RD) or Registered Dietitian Nutritionists (RDN) adhering to the Commission of Dietetic Registration guidelines.</description>
								<pubDate>Tue, 14 Apr 2026 12:45:39 -0400</pubDate>
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									<link>https://careers.chpa.org/jobs/rss/22182071/clinical-dietitian-peds-intestinal-rehab-tpn</link>
								
								<title>Clinical Dietitian Peds Intestinal Rehab/TPN | Duke University and Duke University Health System</title>								
								<guid isPermaLink="true">https://careers.chpa.org/jobs/rss/22182071/clinical-dietitian-peds-intestinal-rehab-tpn</guid>
								<description>Durham, North Carolina,  Clinical Dietitian Peds Intestinal Rehab/TPN 
 &#xa0; 
 Job Code: &#xa0;5034 
 FLSA: &#xa0;E 
 Job Level: &#xa0;F1 
 Supervisory Responsibility: &#xa0;No 
 &#xa0; 
 &#xa0; 
 **Work schedule is Monday through Friday, with weekends on a rotating schedule. After the 90?day probationary period, you will be eligible to work from home one day per week. ** 
 &#xa0; 
 &#xa0; 
 ** This role is part of the pediatric liver transplant and intestinal rehabilitation programs. The focus is on the assessment and management of complex nutrition needs, including enteral and parenteral nutrition support, in collaboration with a multidisciplinary team.&#xa0; Experience with pediatric nutrition support and Certified Nutrition Support Clinician (CNSC) credentialing is preferred. ** 
 &#xa0; 
 &#xa0; 
 General Description of the Job Class 
 Coordinate all phases of nutrition care including nutrition assessment, care planning, monitoring, education and counseling of hospitalized patients and outpatients in a variety of settings. Perform duties in support of and in compliance with performance improvement plans, JCAHO, and other licensing, accrediting, and regulatory agencies. The Duke University Health System offers career advancement through a clinical ladder program. 
 &#xa0; 
 Duties and Responsibilities of this Level 
 Level I 
 Duties and responsibilities may include providing nutrition services and medical nutrition therapy integrated with the patient&#39;s medical goals. Evaluating, interpreting, monitoring and documenting the nutritional status and nutritional needs of hospitalized patients and out patients using established standards of care and practice guidelines. 
 Identifying and providing age-specific nutrition counseling to meet the cultural needs of the patients and their families. 
 Developing, reviewing, updating and implementing educational materials to meet the needs of patients and professionals. 
 Writing orders for diet, supplement, enteral/parenteral nutrition and laboratory data per hospital policy. 
 Functioning as an integral member of the clinical interdisciplinary team. 
 Maintaining registered dietitian (RD) status including continuing professional education per the Professional Development Portfolio. Maintains North Carolina Board of Nutrition and Dietetics licensure. Precepting dietetic interns and provide on the job training for newly hired clinical staff. 
 Supervising daily work of dietetic technicians, registered; provide input into evaluation but doesn&#39;t directly evaluate their performance. Complying with Nutrition Services meeting and attendance standards. 
 &#xa0; 
 Level II 
 In addition to Level I, Dietitian works in an assigned specialty area and integrates research and education into practice as evidence by competencies. Is a liaison and advocate for the profession by utilizing and sharing new practice knowledge and skill into other areas of the profession (management, public health) and or other disciplines. 
 &#xa0; 
 Level III 
 Thinks critically, displays a range of highly developed clinical and technical skills, and formulates judgements acquired through a combination of education, experience and critical thinking. Based on department&#39;s need have the ability to provide expertise, oversight and leadership in a designated specialty area. 
 These areas include: Student Advisor, Malnutrition Specialist, Adult Nutrition Support Specialist, Pediatric Nutrition Support Specialist, Program Coordinator, Clinical and Quality Specialist, IT Specialist, Outpatient Clinical Coordinator, Lead, Subject Matter Expert. 
 Additional information can be found in the DUHS Clinical Dietitian Clinical Ladder Program. 
 &#xa0; Required Qualifications at this Level 
 Education 
 Level I, II, III 
 Baccalaureate degree in Food and Nutrition, Dietetics, Nutritional Sciences, Human Nutrition, or comparable major. 
 Successful completion of coordinated program or dietetic internship of not less than 900 hours under the supervision of a Registered Dietitian. 
 &#xa0; 
 Experience 
 Level I 
 One year in an acute care environment preferred; experience may be waived for specific positions. 
 &#xa0; 
 Level II and Level III 
 At least 5 years of clinical experience or at least 3 years&#39; clinical experience plus an approved, nutrition related certification. 
 &#xa0; 
 Degrees, Licensure, and/or Certification 
 Level I, II, and III 
 Registered dietitian (RD) by the Commission on Dietetic Registration; candidates eligible for registration may be hired with the expectation that registration will be achieved within 90 days of hire. 
 &#xa0; 
 Licensed dietitian/nutritionist (LDN) by the North Carolina Board of Dietetics and Nutrition; provision for license-eligible dietitians as above. 
 &#xa0; 
 Knowledge, Skills, and Abilities 
 Distinguishing Characteristics of this Level 
 N/A 
 &#xa0;</description>
								<pubDate>Tue, 07 Apr 2026 10:51:36 -0400</pubDate>
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									<link>https://careers.chpa.org/jobs/rss/22184151/clinical-dietitian-health-fitness-center</link>
								
								<title>Clinical Dietitian - Health &#38; Fitness Center | Duke University Health System</title>								
								<guid isPermaLink="true">https://careers.chpa.org/jobs/rss/22184151/clinical-dietitian-health-fitness-center</guid>
								<description>Durham, North Carolina,  &#xa0; Clinical Dietitian Part-time at the Duke Health and Fitness Center Work Address:&#xa0;  Duke Health and Fitness Center 3475 Erwin Rd. Durham NC 27705 &#xa0; **Work Schedule is 10am -7pm Mondays + 7 am -3 pm Thursdays**  Some flexibility availability with telehealth work from home options.** &#xa0; The Duke Health &#38; Fitness Center , a medically based wellness center&#xa0;in Durham, NC is seeking a Dietitian to join our nutrition team. &#xa0;Individual nutritional counseling experience in the field of&#xa0;intuitive/mindful eating, HAES, and disordered eating &#xa0;specialties required.&#xa0; Duties include providing nutrition services and medical nutrition therapy integrated with client?s medical goals. &#xa0;Identify and provide age-specific nutrition counseling to meet the cultural needs of the clients and their families. &#xa0;Develop, review, update and implement educational materials to meet the needs of clients and professionals. &#xa0;Maintain registered dietitian (RD) status including continuing professional education per the Professional Development Portfolio &#xa0; General Description of the Job Class Coordinate all phases of nutrition care including nutrition assessment, care planning, monitoring, education and counseling of hospitalized patients and outpatients in a variety of settings. Perform duties in support of and in compliance with performance improvement plans, JCAHO, and other licensing, accrediting, and regulatory agencies. The Duke University Health System offers career advancement through a clinical ladder program. &#xa0; Duties and Responsibilities of this Level Level I Duties and responsibilities may include providing nutrition services and medical nutrition therapy integrated with the patient&#39;s medical goals. Evaluating, interpreting, monitoring and documenting the nutritional status and nutritional needs of hospitalized patients and out patients using established standards of care and practice guidelines. Identifying and providing age-specific nutrition counseling to meet the cultural needs of the patients and their families. Developing, reviewing, updating and implementing educational materials to meet the needs of patients and professionals. Writing orders for diet, supplement, enteral/parenteral nutrition and laboratory data per hospital policy. Functioning as an integral member of the clinical interdisciplinary team. Maintaining registered dietitian (RD) status including continuing professional education per the Professional Development Portfolio. Maintains North Carolina Board of Nutrition and Dietetics licensure. Precepting dietetic interns and provide on the job training for newly hired clinical staff. Supervising daily work of dietetic technicians, registered; provide input into evaluation but doesn&#39;t directly evaluate their performance. Complying with Nutrition Services meeting and attendance standards. &#xa0; Level II In addition to Level I, Dietitian works in an assigned specialty area and integrates research and education into practice as evidence by competencies. Is a liaison and advocate for the profession by utilizing and sharing new practice knowledge and skill into other areas of the profession (management, public health) and or other disciplines. &#xa0; Level III Thinks critically, displays a range of highly developed clinical and technical skills, and formulates judgements acquired through a combination of education, experience and critical thinking. Based on department&#39;s need have the ability to provide expertise, oversight and leadership in a designated specialty area. These areas include: Student Advisor, Malnutrition Specialist, Adult Nutrition Support Specialist, Pediatric Nutrition Support Specialist, Program Coordinator, Clinical and Quality Specialist, IT Specialist, Outpatient Clinical Coordinator, Lead, Subject Matter Expert. Additional information can be found in the DUHS Clinical Dietitian Clinical Ladder Program. &#xa0; Required Qualifications at this Level Education Level I, II, III Baccalaureate degree in Food and Nutrition, Dietetics, Nutritional Sciences, Human Nutrition, or comparable major. Successful completion of coordinated program or dietetic internship of not less than 900 hours under the supervision of a Registered Dietitian. &#xa0; Experience Level I One year in an acute care environment preferred; experience may be waived for specific positions. &#xa0; Level II and Level III At least 5 years of clinical experience or at least 3 years&#39; clinical experience plus an approved, nutrition-related certification. &#xa0; Degrees, Licensure, and/or Certification Level I, II, and III Registered dietitian (RD) by the Commission on Dietetic Registration; candidates eligible for registration may be hired with the expectation that registration will be achieved within 90 days of hire. Licensed dietitian/nutritionist (LDN) by the North Carolina Board of Dietetics and Nutrition; provision for license-eligible dietitians as above. &#xa0; Knowledge, Skills, and Abilities N/A &#xa0; Distinguishing Characteristics of this Level N/A Job Code: 00005034 CLINICAL DIETITIAN Job Level: F1 &#xa0; Duke is an Affirmative Action/Equal Opportunity Employer committed to providing employment opportunity without regard to an individual&#39;s age, color, disability, gender, gender expression, gender identity, genetic information, national origin, race, religion, sex, sexual orientation, or veteran status. &#xa0; Duke aspires to create a community built on collaboration, innovation, creativity, and belonging. Our collective success depends on the robust exchange of ideas-an exchange that is best when the rich diversity of our perspectives, backgrounds, and experiences flourishes. To achieve this exchange, it is essential that all members of the community feel secureand welcome, that the contributions of all individuals are respected, and that all voices are heard. All members of our community have a responsibility to uphold these values. &#xa0; Essential Physical Job Functions: Certain jobs at Duke University and Duke University Health System may include essential job functions that require specific physical and/or mental abilities. Additional information and provision for requests for reasonable accommodation will be provided by each hiring department. &#xa0;</description>
								<pubDate>Fri, 24 Apr 2026 00:58:08 -0400</pubDate>
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									<link>https://careers.chpa.org/jobs/rss/22217735/regulatory-compliance-assistant</link>
								
								<title>Regulatory Compliance Assistant | The Ohio State University</title>								
								<guid isPermaLink="true">https://careers.chpa.org/jobs/rss/22217735/regulatory-compliance-assistant</guid>
								<description>,  Regulatory Compliance Assistant to provide support to assure research protocols are in compliance with university, state and federal regulations across research groups managed by the College of Medicines Center for Clinical Research Management (CCRM); assists with regulatory functions in support of clinical research activity; assists in preparation of protocol submissions to Institutional Review Boards (IRBs) and provides updates on submission status; assists in preparation of other required regulatory documents; distributes approved documents; relays information to clinical research staff; assists with data entry including collecting, entering and maintaining data and documents in the OnCore electronic database and e-Regulatory; assists with monitoring visits; assists with regulatory issues; creates and maintains regulatory files. Minimum Education Required High School diploma or GED. Certification or vocational training may be preferred.  Preferred Education Bachelor&#39;s degree, preferably in biological sciences, health sciences, or life sciences Required Experience 1 year of relevant experience required.  Preferred Experience 2-4 years of relevant experience preferred.  Experience in a clinical research capacity desired; computer skills required with knowledge of database software applications desired. Requires successful completion of a background check.  Selected candidate may be requested to complete a pre-employment physical including a drug screen.    FUNCTION/SUBFUNCTION: Research Administration/Research Compliance  CAREER BAND: Individual Contributor-Technical  CAREER LEVEL: T2                                                                                  This is a hyrbrid position with the majority of job duties being able to be completed remotely; however, individuals may need to come to the office for specific trainings, group meetings/gatherings, etc.</description>
								<pubDate>Fri, 24 Apr 2026 02:33:33 -0400</pubDate>
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									<link>https://careers.chpa.org/jobs/rss/22077265/research-assistant-safety-x28-neurology-x29</link>
								
								<title>Research Assistant, Safety &#38;#x28;Neurology&#38;#x29; | Johns Hopkins University</title>								
								<guid isPermaLink="true">https://careers.chpa.org/jobs/rss/22077265/research-assistant-safety-x28-neurology-x29</guid>
								<description>Baltimore, Maryland,  The Department of Neurology is seeking a  Research Assistant  to provide administrative and technical support for research safety activities, including documentation, data tracking, quality procedures, and coordination across research studies for the BIOS Clinical Trials Coordinating Center. The Research Assistant oversees data collection, data organization, and/or data management or similar functions/tasks for research study(ies) in support of a PI or a research team. Specific Duties &#38; Responsibilities  Run routine and ad hoc reports.  Use standard tools and computer programs to review data.  Assist with data cleaning measures to ensure accuracy of data and preparation of tables.  Lead basic activities such as data collection and data entry.  May lead specific tasks and develop processes to ensure study activities occur effectively and efficiently.  May conduct literature searches to support faculty in research efforts.  May design and format papers/publications.  May assist PIs in writing summaries of papers for release as policy briefs or other channels. Other duties as assigned. In addition to the duties described above Coordinate materials, records, and communications across research teams. Support quality control activities and adherence to established procedures. Perform routine data entry, tracking, and basic reporting in research systems. Assist with maintaining safety, regulatory, and study documentation. Support research safety and monitoring activities for ongoing studies. Minimum Qualifications Bachelor&#39;s Degree in a related field. Additional education may substitute for required experience and additional related experience may substitute for required education beyond a high school diploma/graduation equivalent, to the extent permitted by the JHU equivalency formula. Preferred Qualifications &#xa0; &#xa0; Classified Title: Research Assistant&#xa0; Job Posting Title (Working Title):&#xa0;Research Assistant, Safety (Neurology)&#xa0;&#xa0;&#xa0; Role/Level/Range: ACRO40/E/03/CD&#xa0;&#xa0; Starting Salary Range: $17.20 - $30.30 HRLY (Commensurate w/exp.)&#xa0; Employee group: Full Time&#xa0; Schedule: M-F 8:30 am - 5:00 pm&#xa0; FLSA Status:&#xa0;Non-Exempt&#xa0; Location: Hybrid/School of Medicine Campus &#xa0; Department name: SOM Neuro BIOS &#xa0; Personnel area: School of Medicine&#xa0; &#xa0; &#xa0;</description>
								<pubDate>Fri, 24 Apr 2026 00:51:05 -0400</pubDate>
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									<link>https://careers.chpa.org/jobs/rss/21990480/dental-assistant-temp</link>
								
								<title>Dental Assistant (Temp) | University of Alabama, Birmingham</title>								
								<guid isPermaLink="true">https://careers.chpa.org/jobs/rss/21990480/dental-assistant-temp</guid>
								<description>Birmingham, Alabama,  Job Description Position Summary The Dental Assistant (Temporary) supports dental providers by assisting with clinical and administrative duties in a fast-paced dental care environment. This role helps ensure efficient patient flow, high-quality patient care, and adherence to UAB and regulatory standards. The ideal candidate is dependable, detail-oriented, and experienced in chairside assistance. Key Responsibilities Assist dentists and dental residents during examinations and procedures Prepare treatment rooms, instruments, and materials prior to patient visits Escort patients to and from treatment areas and ensure patient comfort Sterilize and maintain dental instruments and equipment in accordance with infection control standards Take and develop dental radiographs as permitted by training and regulations Maintain accurate patient records and documentation in dental or electronic health record systems Assist with patient education and post-procedure instructions Follow all UAB safety, HIPAA, and infection control policies Perform general clinic support duties as needed to support daily operations   Hourly Rate: $16.50 Qualifications Required Qualifications High school diploma or GED Prior experience as a Dental Assistant or in a dental clinical setting Knowledge of dental instruments, procedures, and infection control practices Strong interpersonal and communication skills Ability to work efficiently in a fast-paced, patient-facing environment Preferred Qualifications Dental Assistant certification or completion of a dental assisting program Experience in an academic, hospital-based, or specialty dental clinic Experience with dental charting systems or electronic health records   UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran&#39;s status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UAB&#39;s Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix. Job:UAB Temporary Services</description>
								<pubDate>Fri, 24 Apr 2026 00:47:04 -0400</pubDate>
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									<link>https://careers.chpa.org/jobs/rss/22055870/dental-assistant-iii-2</link>
								
								<title>DENTAL ASSISTANT III (2) | University of Alabama, Birmingham</title>								
								<guid isPermaLink="true">https://careers.chpa.org/jobs/rss/22055870/dental-assistant-iii-2</guid>
								<description>Birmingham, Alabama,  Job Description The University of Alabama at Birmingham (UAB) seeks a DENTAL ASSISTANT III to be responsible for providing support in various dental procedures, assisting with surgical procedures, sedation, and anesthesia. Maintains surgery rooms and equipment, takes and processes radiographs of patients and dispenses supplies. Assists residents and faculty with anesthesia of all types to include conscious sedation, IV sedation, nitrous oxide and general anesthesia. Obtains patient consent. Attaches and detaches patient to monitor to access blood pressure, heart rate and oxygen saturation, recognizes abnormal readings and reports problems to resident/faculty surgeon. Charts patient vital signs throughout procedure. Verbally communicates pre-operative and post-operative instructions to patient. Performs a variety of clerical and administrative duties in support of department. Answers phones, takes messages and makes appointments, explains and receives payment for procedures, etc. Responds to the unique needs of all patients ages newborn to geriatric.  RESPONSIBILITIES: Assists residents and students during examinations and procedures, including surgeries; prepares treatment rooms for patient care; takes and develops dental radiographs (X-rays); and sterilizes and maintains dental instruments and equipment. Maintain inventory and order supplies and equipment while updating a shared tracking spreadsheet. Ensure quality assurance and regulatory compliance within the clinic. Schedule patient appointments and manage the front desk to ensure a high-quality patient experience. Perform other duties as assigned. (Hourly Rate: $16.00 - $26.00) Qualifications Graduate from an accredited Dental Assistant Program and two (2) years of related experience required. Work experience may substitute for education requirement.  Experienced dental assistant with strong knowledge and skills in assisting with dental surgeries, managing inventory, coordinating patient scheduling, and providing post-operative care instructions. Experience in Endodontics is preferred. Preferred hard skills: Include proficiency in Microsoft Excel, operation of standard dental equipment, and proper sterilization of dental instruments. Candidates should also be familiar with dental clinic operations, including quality assurance processes, regulatory requirements, and front desk management. Microsoft Excel, operating most dental equipment, and sterilization of dental instruments. Familiar with dental clinic operations to include quality assurance, regulatory requirements and front desk management.           UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran&#39;s status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UAB&#39;s Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix. Job:Clerical %26 Administrative</description>
								<pubDate>Fri, 24 Apr 2026 00:47:04 -0400</pubDate>
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									<link>https://careers.chpa.org/jobs/rss/22226257/certified-medical-assistant-family-medicine-brevard-prn</link>
								
								<title>Certified Medical Assistant Family Medicine Brevard PRN | AdventHealth</title>								
								<guid isPermaLink="true">https://careers.chpa.org/jobs/rss/22226257/certified-medical-assistant-family-medicine-brevard-prn</guid>
								<description>Brevard, North Carolina,  Our promise to you: Joining AdventHealth is about being part of something bigger. It&#8217;s about belonging to a community that believes in the wholeness of each person, and serves to uplift others in body, mind and spirit. AdventHealth is a place where you can thrive professionally, and grow spiritually, by Extending the Healing Ministry of Christ. Where you will be valued for who you are and the unique experiences you bring to our purpose-minded team. All while understanding that  together  we are even better. Schedule:  PRN Shift: Day (United States of America) Address: 123 E Main St City: Brevard State: North Carolina Postal Code: 28712 Job Description: Shift:  PRN (Providing coverage for 2 offices) Location : 22 Trust Ln. Brevard, NC 123 E. Main Street Brevard, NC&#xa0; Suite 102 Travels as needed to fulfill staffing needs and support clinic operations. Stays up to date and familiar with all policies and procedures, ensuring compliance with organizational standards. Maintains education requirements for the position and demonstrates competency through annual clinical competencies and written tests. Ensures efficient office flow by preparing patients and equipment for treatment, initiating testing, and documenting results in the practice&#8217;s designated system. Maintains OSHA regulatory enforcement and other office compliance, following safety processes and policies. Provides whole care to patients during office visits, including intake, test results, screenings, labs, medication administration, and closure of care gaps. Maintains confidentiality of employees&#38;#39; and patients&#38;#39; administrative and medical information. Supports staff teamwork by assisting patients, visitors, and co-workers when necessary. Performs clinical intake according to policy and procedures, including screenings, history taking, vital signs, and medication reconciliation. Assists with minor procedures associated with specialty and ensures accurate documentation at the time of service or results. Educates patients regarding tests, medications, and diet, providing clear and accurate instructions. Monitors and manages inventory, ensuring adequate supplies and functioning medical equipment. Performs other duties as assigned. Knowledge, Skills, and Abilities: &#8226; Knowledge of health care field and medical terminology [Required] &#8226; Knowledge of chronic disease management [Required] &#8226; Knowledge of and ability to utilize internal and external resources [Required] &#8226; Expertise in patient advocacy and navigating complex systems [Required] &#8226; Ability to function and assist others in stressful, fast-paced environments and effectively apply stress management techniques [Required] &#8226; Ability to resolve issues and work independently within the scope of their certification [Required] &#8226; Ability to exercise sound judgement, diplomacy and a professional demeanor [Required] &#8226; Demonstrates ability to communicate by reading, writing and typing legibly, speaking and comprehending English effectively to carry out job requirements [Required] &#8226; Experience with computers required [Required] Education: &#8226; High School Grad or Equiv [Required] Field of Study: &#8226; N/A Work Experience: &#8226; 1&#38;#43; year of related work experience [Preferred] Additional Information: &#8226; N/A Licenses and Certifications: &#8226; Basic Life Support - CPR Cert (BLS) [Required] &#8226; American Association Medical Assistants (CMA) [Required]  OR  Clinical Medical Assistant Certification (CMAC) [Required]  OR  Registered Medical Assistant (RMA) [Required]  OR  National Certified Medical Assistant (NCMA) [Required]  OR  Certified Clinical Medical Assistant (CCMA) [Required]  OR  Nationally Registered Certified Medical Assistant (NRCMA) [Required] Physical Requirements:  (Please click the link below to view work requirements) Physical Requirements - https://tinyurl.com/msy4mja2 Pay Range: $16.42 - $26.27 This facility is an equal opportunity employer and complies with federal, state and local anti-discrimination laws, regulations and ordinances.</description>
								<pubDate>Fri, 24 Apr 2026 01:16:34 -0400</pubDate>
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									<link>https://careers.chpa.org/jobs/rss/22226185/medical-assistant-prn</link>
								
								<title>Medical Assistant PRN | AdventHealth</title>								
								<guid isPermaLink="true">https://careers.chpa.org/jobs/rss/22226185/medical-assistant-prn</guid>
								<description>Venice, Florida,  Our promise to you: Joining AdventHealth is about being part of something bigger. It&#8217;s about belonging to a community that believes in the wholeness of each person, and serves to uplift others in body, mind and spirit. AdventHealth is a place where you can thrive professionally, and grow spiritually, by Extending the Healing Ministry of Christ. Where you will be valued for who you are and the unique experiences you bring to our purpose-minded team. All while understanding that  together  we are even better. Schedule:  PRN Shift: Day (United States of America) Address: 1201 JACARANDA BLVD City: VENICE State: Florida Postal Code: 34292 Job Description: Travels as needed to fulfill staffing needs and support clinic operations. Stays up to date and familiar with all policies and procedures, ensuring compliance with organizational standards. Maintains education requirements for the position and demonstrates competency through annual clinical competencies and written tests. Ensures efficient office flow by preparing patients and equipment for treatment, initiating testing, and documenting results in the practice&#8217;s designated system. Maintains OSHA regulatory enforcement and other office compliance, following safety processes and policies. Provides whole care to patients during office visits, including intake, test results, screenings, labs, medication administration, and closure of care gaps. Maintains confidentiality of employees&#38;#39; and patients&#38;#39; administrative and medical information. Supports staff teamwork by assisting patients, visitors, and co-workers when necessary. Performs clinical intake according to policy and procedures, including screenings, history taking, vital signs, and medication reconciliation. Assists with minor procedures associated with specialty and ensures accurate documentation at the time of service or results. Educates patients regarding tests, medications, and diet, providing clear and accurate instructions. Monitors and manages inventory, ensuring adequate supplies and functioning medical equipment. Performs other duties as assigned. Knowledge, Skills, and Abilities: &#8226; Knowledge of health care field and medical terminology [Required] &#8226; Knowledge of chronic disease management [Required] &#8226; Knowledge of and ability to utilize internal and external resources [Required] &#8226; Expertise in patient advocacy and navigating complex systems [Required] &#8226; Ability to function and assist others in stressful, fast-paced environments and effectively apply stress management techniques [Required] &#8226; Ability to resolve issues and work independently within the scope of their certification [Required] &#8226; Ability to exercise sound judgement, diplomacy and a professional demeanor [Required] &#8226; Demonstrates ability to communicate by reading, writing and typing legibly, speaking and comprehending English effectively to carry out job requirements [Required] &#8226; Experience with computers required [Required] Education: &#8226; High School Grad or Equiv [Required] Field of Study: &#8226; N/A Work Experience: &#8226; 1&#38;#43; year of related work experience [Preferred] Additional Information: &#8226; N/A Licenses and Certifications: &#8226; Basic Life Support - CPR Cert (BLS) [Required] &#8226; American Association Medical Assistants (CMA) [Required]  OR  Clinical Medical Assistant Certification (CMAC) [Required]  OR  Registered Medical Assistant (RMA) [Required]  OR  National Certified Medical Assistant (NCMA) [Required]  OR  Certified Clinical Medical Assistant (CCMA) [Required]  OR  Nationally Registered Certified Medical Assistant (NRCMA) [Required] Physical Requirements:  (Please click the link below to view work requirements) Physical Requirements - https://tinyurl.com/msy4mja2 Pay Range: $17.11 - $27.38 This facility is an equal opportunity employer and complies with federal, state and local anti-discrimination laws, regulations and ordinances.</description>
								<pubDate>Fri, 24 Apr 2026 01:16:34 -0400</pubDate>
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									<link>https://careers.chpa.org/jobs/rss/22151020/assistant-program-director-ehs-ccp-manager</link>
								
								<title>Assistant Program Director (EHS-CCP Manager) | Tennessee State University</title>								
								<guid isPermaLink="true">https://careers.chpa.org/jobs/rss/22151020/assistant-program-director-ehs-ccp-manager</guid>
								<description>Nashville, Tennessee,  Job Description:   Tennessee State University Office of  COE  Learning Sciences&#xa0; invites applications for the role of  Assistant Program Director (Early Head Start &#8211; Child Care Partnerships Manager) .  Nature of Work: Assist Program Director in overseeing all aspects of the  EHS  program. Serve as manager of the  EHS - CCP  program. Hours of work and schedule are determined based upon program needs and availability of funds. The Assistant Program Director is based at the  TSU   COE -LS main office and travel within the multi-county service area is required. Valid TN Driver License and reliable transportation required. Will be required to travel within a four-county service area. Essential Job Responsibilities: Budget, Grants, and Facility Development Oversee program budgets and purchases. Participate in the development of collaborations and facility development for future expansion of families and/or services. Present financial reports for Board of Directors and Policy Council. Assist in the coordination of annual grant application process. Assist with data analysis and summarizing of annual self-assessment and develop service plans in response to findings. Systems Evaluation, Monitoring, Compliance and Development Assist in the design of internal structures, systems, and policies. Assist in strategic planning process and the development of Work Plans. Facilitate community needs assessments. Ensure adequate systems are in place to maintain the highest quality of services to children and families in compliance with Head Start Program Performance Standards, Head Start Act and Tennessee licensing Ensure consistency in service delivery across programs with attention to inclusive practices and integration of component areas. Assist in the completion of the annual Self-Assessment and Community Assessment as required by Head Start regulations. Communication/Public Relations Establish and maintain effective working relationships with the members of the Board of Directors, Policy Council, and Growing Futures staff. Establish and maintain relationships and collaborations with public school districts, systems of higher education, and other community agencies and partners. Collaborate with community agencies to advocate for the needs of  TSU   EHS  children and families. Promote a consistent exchange of information in all directions. Attend Tennessee Head Start Association ( THSA ) Director meetings as scheduled. Prepare and submit program annual report to public annually. Prepare and submit  EHS  program reports for Board of Directors and Policy Council, Head Start organizations, Region IV office as needed. Prepare and submit annual Program Information Report ( PIR ). Supervisory Responsibilities In collaboration with  EHS - CCP  directors/owners, establish and maintain regular oversight of  EHS - CCP  centers. Conduct  EHS - CCP  Director meetings. Facilitate resolutions of conflicts. Characteristics and Skills: Mature, responsible individual who has experience in leadership and management, preferably in a child development program, including services to children with special needs. Motivating staff and providing training to individuals in order to maintain quality. Ability to balance regulatory requirements with budget constraints and growing community needs. Knowledge of state, regional and local based resources required. Knowledge of Head Start Performance Standards preferred. Strong leadership skills and the ability to make decisions based on policies and procedures. Additional Responsibilities Responsible for general knowledge of state and federal regulations. Encourage and support professional development opportunities of program staff. Follow  TSU  policy in work conduct including but not limited to travel, attendance, outside employment, etc. Maintain the Early Head Start policy manual and keep up-to-date. Other duties assigned Program Director and Research and Sponsored Programs Director.</description>
								<pubDate>Fri, 24 Apr 2026 02:16:53 -0400</pubDate>
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									<link>https://careers.chpa.org/jobs/rss/22225009/clinical-research-coordinator-ii</link>
								
								<title>CLINICAL RESEARCH COORDINATOR II | University of Alabama, Birmingham</title>								
								<guid isPermaLink="true">https://careers.chpa.org/jobs/rss/22225009/clinical-research-coordinator-ii</guid>
								<description>Birmingham, Alabama,  Job Description The University of Alabama at Birmingham (UAB), School of Medicine, Division of Clinical Immunology and Rheumatology, is seeking a Clinical Research Coordinator II to conduct the following: screening and enrolling participants in rheumatology observational studies and clinical trials, conduct informed consent per GCP guidelines, conduct patient screening and enrollment, conduct patient visits per protocol, document adverse events, medications, and procedures conducted at each visit, prepare lab kits for each patient visit, administer study questionnaires, and other procedures as trained. The CRC II will compile and analyze data, develop and implement procedures, maintain records, track progress, and conduct quality assurance on data collected. This position will serve as a mentor to junior staff, conduct protocol training, assist PIs to develop regulatory protocols and documents, and attend team meetings and educational training as required. General Responsibilities To serve as coordinator for studies and provide support to other team members within the confines of the protocol as directed. To support screening and participant eligibility determination, working with more senior team members to ensure compliance. To conduct activities in accordance with the protocol, regulations and Good Clinical Practice (GCP). To assist with the study life cycle from start-up to closure, i.e., collecting and recording data, recruiting and performing follow-up with participants, scheduling visits and assisting in coordination of lab and fieldwork. Key Duties &#38; Responsibilities Screens and enrolls participants in Rheumatology clinical research studies and trials. Conducts patient visits per protocol schedule of events. Documents adverse events, medications, and procedures conducted at each visit. Works with sponsors and PI to address study data queries. Assists the PI in developing protocol documents, manuals, and reports. Attends team meetings and educational training as required. In conjunction with Investigators, plans and implements the clinical protocol&#39;s goals and objectives. Compiles and edits written reports for both internal and external administrative offices. Serves as a mentor to junior staff, including student assistants. Performs other duties as assigned. Annual Salary Range :     $50,050 - $81,330 Qualifications Bachelor&#39;s degree in a related field and three (3) years of related experience required.  Work experience may substitute for education requirement.    UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran&#39;s status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UAB&#39;s Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix. Job:Clinical Research</description>
								<pubDate>Fri, 24 Apr 2026 00:47:04 -0400</pubDate>
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									<link>https://careers.chpa.org/jobs/rss/22225008/clinical-research-coordinator-ii</link>
								
								<title>CLINICAL RESEARCH COORDINATOR II | University of Alabama, Birmingham</title>								
								<guid isPermaLink="true">https://careers.chpa.org/jobs/rss/22225008/clinical-research-coordinator-ii</guid>
								<description>Birmingham, Alabama,  Job Description The University of Alabama at Birmingham (UAB), School of Medicine, Division of Clinical Immunology and Rheumatology, is seeking a Clinical Research Coordinator II to conduct the following: screening and enrolling participants in rheumatology observational studies and clinical trials, conduct informed consent per GCP guidelines, conduct patient screening and enrollment, conduct patient visits per protocol, document adverse events, medications, and procedures conducted at each visit, prepare lab kits for each patient visit, administer study questionnaires, and other procedures as trained. The CRC II will compile and analyze data, develop and implement procedures, maintain records, track progress, and conduct quality assurance on data collected. This position will serve as a mentor to junior staff, conduct protocol training, assist PIs to develop regulatory protocols and documents, and attend team meetings and educational training as required. General Responsibilities To serve as coordinator for studies and provide support to other team members within the confines of the protocol as directed. To support screening and participant eligibility determination, working with more senior team members to ensure compliance. To conduct activities in accordance with the protocol, regulations and Good Clinical Practice (GCP). To assist with the study life cycle from start-up to closure, i.e., collecting and recording data, recruiting and performing follow-up with participants, scheduling visits and assisting in coordination of lab and fieldwork. Key Duties &#38; Responsibilities Screens and enrolls participants in Rheumatology clinical research studies and trials. Conducts patient visits per protocol schedule of events. Documents adverse events, medications, and procedures conducted at each visit. Works with sponsors and PI to address study data queries. Assists the PI in developing protocol documents, manuals and reports. Attends team meetings and educational training as required. In conjunction with Investigators, plans and implements the clinical protocol&#39;s goals and objectives. Compiles and edits written reports for both internal and external administrative offices. Serves as a mentor to junior staff, including student assistants. Performs other duties as assigned. Annual Salary Range :     $50,050 - $81,330 Qualifications Bachelor&#39;s degree in a related field and three (3) years of related experience required.  Work experience may substitute for education requirement.   UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran&#39;s status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UAB&#39;s Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix. Job:Clinical Research</description>
								<pubDate>Fri, 24 Apr 2026 00:47:04 -0400</pubDate>
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									<link>https://careers.chpa.org/jobs/rss/22156045/small-farms-extension-research-associate-2-spanish-or-chinese-bilingual-riverside-san-diego-ca-job-id-85209</link>
								
								<title>Small Farms Extension &#38; Research Associate 2 (Spanish or Chinese Bilingual)  Riverside / San Diego, CA, Job ID 85209 | University of California Agriculture and Natural Resources</title>								
								<guid isPermaLink="true">https://careers.chpa.org/jobs/rss/22156045/small-farms-extension-research-associate-2-spanish-or-chinese-bilingual-riverside-san-diego-ca-job-id-85209</guid>
								<description>San Diego, California,  Small Farms Extension &#38; Research Associate 2 (Korean, Chinese, or Spanish Bilingual)  San Diego / Riverside, CA, Job ID 85209 University of California Agriculture and Natural Resources Job Description      Position Summary: The Small Farms Extension and Research Associate will assist UC ANR Small Farms Advisors in the delivery of technical assistance, training, outreach, and applied research activities to increase extension support for small-scale, diversified, and historically underserved farmers. Areas of focus include on-farm production challenges such as irrigation, nutrient management, and pest management; regulatory compliance; marketing and business support; and incentive program and grant application technical support. Working under the general direction of a county-based Small Farms Advisor, the Associate assists UC ANR academics, staff, and collaborating growers with collection and analysis of data needed for grower surveys, applied research projects, program development and evaluation, and policy communications. The Associate will also provide expert, technical assistance in English, as well as Korean, Chinese, or Spanish to small-scale farmers to enhance on-farm productivity, compliance with local, state, and federal regulatory programs, and access to resources such as grants, incentives programs, and emergency relief programs. The Associate will assist UC ANR academics in the extension of applied research results and the development, delivery, and evaluation of bilingual, culturally appropriate, research-based educational materials and extension programming to support small-scale, diversified, and historically underserved farmers. The Associate will develop and conduct effective methods to increase outreach and participate in program evaluation, needs assessments, and strategic planning for outreach and extension efforts in the assigned county or counties. Applied research duties include assisting with survey development and translation, recruitment of farmer participants, setup of field experiments, data collection and management, basic data analysis for outreach, educational programming, and research projects. Research, outreach, and extension efforts will also be coordinated with a statewide network of Small Farms Advisors and program staff in multiple counties. The Small Farms Network will work closely with partner agencies and non-profit organizations to coordinate and leverage statewide technical assistance efforts. The position requires regular travel to farms within assigned counties, including remote and rural areas, a minimum of two days per week as needed, and occasional travel outside the assigned counties. This position will cover Riverside and San Diego Counties. Office Location - The selected candidate may choose either the Riverside or San Diego office as their office location, contingent upon space availability and approval of the County Director. If the San Diego office is selected, in addition to the two days a week spent traveling to farms, the employee will also be required to report to the Riverside office once a week to work directly with the Riverside team. If the Riverside office location is selected, in addition to the two days a week spent traveling to farms, the employee will also attend monthly in-person staff meetings in San Diego. This position is a career appointment that is 100% fixed.  Pay Scale:  $31.23 /hour to $39.60/hour Job Posting Close Date:  This job is open until filled. The first application review date will be 4/15/2026. Key Responsibilities: 75%    Provide growers with direct, one-on-one, bilingual technical assistance and extension support. Travel to farms, conduct farm visits and meet with farmers individually to assist with production challenges, marketing, regulatory compliance, and access to grants, incentives, and economic relief programs. Assist farmers with online applications and collect data to identify barriers to access to programs.    Assist with survey development and data collection for county-level and statewide needs assessments to inform strategic planning of outreach, training, and applied research efforts. Assist with translation and review of survey questions. Assist with recruitment of survey participants.    Collect and organize evaluation data from participants at workshops and individual farm visits. Gather input from farmers and conduct basic analyses of data to inform program improvements.    Organize and maintain electronic records such as farmer contact lists and coordinate bilingual outreach through radio, social media, newsletters, farm visits, and networking. Organize, promote, and assist with extension workshops on a range of research, extension, and technical assistance topics.    Gather data to inform policy discussions, including feedback from partner organizations, and summarize results for policy communications. Develop and deliver presentations at meetings with nonprofit partner organizations, regulatory agencies, and policy makers to provide research-based information on the needs and challenges of small-scale farms and to develop new collaborations.    Develop and design bilingual educational materials and deliver educational programming to assist small-scale farmers in accessing markets and assistance programs, complying with regulations in areas such as food safety, labor, groundwater use, fertilizer use, pesticide use, and organic certification, and addressing crop production challenges through improved irrigation, nutrient management, pest management, and other production practices.    Serve as a lead worker on multi-county outreach and technical assistance efforts where background and expertise are sufficient to serve as a subject matter expert for specific project topics.    Collect soil, plant, insect, water, and other types of samples to assist with research and technical support activities. 15%    Assist the Small Farms Advisor with research activities and data management, including data collection for field research trials. Travel to field research sites to complete activities.    Keep accurate and timely records and develop systems to organize reporting data. Manage database and Excel records, assist with tracking of activities, farmer contacts, and expenses, organize information for program evaluation, and prepare data summaries.    Conduct basic data analysis on demographic, survey, and field trial data.    Provide oral and written reports on a regular basis on data collection and results.    Assist in development of reports as required by funding agencies and internal reporting procedures. 10%    Provide coordination and bilingual support for outreach projects with growers, such as on-farm demonstrations and tailgate meetings.    Order supplies for research and extension projects.    Prepare equipment and supplies necessary for field work and data collection.    Recruit farmers to participate in on-farm research trials and assist with translation and communication to facilitate research activities.    Coordinate logistics necessary for data collection with county office staff and other research assistants.    Keep academics, staff, and other project collaborators informed of data collection status, pertinent results, and issues affecting research projects.    Travel to farms to conduct outreach, training, and research activities. Requirements: A minimum of a Bachelor&#39;s degree with coursework in the agricultural or social sciences relevant to agricultural extension, applied research, and community engagement and/or equivalent experience or training. Excellent organizational skills to collect data and maintain integrity of data.  Ability to pay attention to details and produce accurate results.  Proficiency in Microsoft Office applications including Word, Excel, and PowerPoint.  Excellent time management skills and the ability to manage multiple project tasks to ensure successful completion. Excellent verbal and written communication and interpersonal skills to communicate complex agronomic, business, and regulatory topics to in a manner understandable to growers. Ability to analyze, evaluate and synthesize information relevant to grower needs and challenges, applications of research results, and policy communications. Experience working in an agricultural setting or directly working with farmers.  Proficient bilingual communication skills including the ability to read, write, translate, and effectively communicate technical agricultural information in a language relevant to growers within the county region served by the position, such as Spanish, Hmong, Chinese, or Korean. This position requires bilingual communication skills in English and Korean, Chinese, or Spanish. Preferred Skills: General knowledge of the biological and natural sciences, including fields such as soils, entomology, and plant physiology and pathology, and/or general knowledge of the social and economic sciences. Working knowledge of basic agricultural research methods and/or experience in applied research.  Experience conducting surveys, focus groups, analysis of demographic data, or other social science research methods. Experience in extension, adult education, project coordination, public speaking, community development, or community outreach. Demonstrated skills and experience communicating research results to diverse audiences.  Experience working with disadvantaged, marginalized, or historically underserved communities. Special Conditions of Employment: Must possess valid California Driver&#39;s License to drive a County or University vehicle. Ability and means to travel on a flexible schedule as needed, proof of liability damage insurance on vehicle used is required. Reimbursement of job-related travel will be reimbursed according to University policies. Ability and means to travel to farms within assigned counties, including remote and rural areas, a minimum of two days per week as needed, and occasional travel outside the assigned counties. Travel including travel outside normal business hours may be requested. Overtime and occasional weekend work as needed, usually on short notice to meet operational needs may be requested. The University reserves the right to make employment contingent upon successful completion of the background check. This is a designated position requiring a background check and may require fingerprinting due to the nature of the job responsibilities. UC ANR does hire people with conviction histories and reviews information received in the context of the job responsibilities. As of January 1, 2014, ANR is a smoke- and tobacco-free environment in which smoking, the use of smokeless tobacco products, and the use of unregulated nicotine products (e-cigarettes), is strictly prohibited. As a condition of employment, you will be required to comply with the University of California  https://apptrkr.com/get_redirect.php?id=7038743&#38;targetURL= Policy on Vaccination Programs , as may be amended or revised from time to time.  Federal, state, or local public health directives may impose additional requirements. Misconduct Disclosure Requirement:   As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer.  a. &#39;Misconduct&#39; means any violation of the policies or laws governing conduct at the applicant&#39;s previous place of employment, including, but not limited to, violations of policies or laws prohibiting sexual harassment, sexual assault, or other forms of harassment, discrimination, dishonesty, or unethical conduct, as defined by the employer.  For reference, below are UC&#39;s policies addressing some forms of misconduct:  UC Sexual Violence and Sexual Harassment Policy  UC Anti-Discrimination Policy   Abusive Conduct in the Workplace      To apply, please visit:  https://careerspub.universityofcalifornia.edu/psc/ucanr/EMPLOYEE/HRMS/c/HRS_HRAM_FL.HRS_CG_SEARCH_FL.GBL?Page=HRS_APP_JBPST_FL&#38;JobOpeningId=85209&#38;PostingSeq=1&#38;SiteId=17&#38;languageCd=ENG&#38;FOCUS=Applicant Copyright 2025 Jobelephant.com Inc. All rights reserved. Posted by the FREE value-added recruitment advertising agency   jeid-b0d9c079a053754e8d33dad39d9634f9</description>
								<pubDate>Fri, 24 Apr 2026 02:26:20 -0400</pubDate>
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									<link>https://careers.chpa.org/jobs/rss/22156044/small-farms-extension-research-associate-2-korean-chinese-or-spanish-bilingual-riverside-ca-job-id-85196</link>
								
								<title>Small Farms Extension &#38; Research Associate 2 (Korean, Chinese, or Spanish Bilingual)  Riverside, CA, Job ID 85196 | University of California Agriculture and Natural Resources</title>								
								<guid isPermaLink="true">https://careers.chpa.org/jobs/rss/22156044/small-farms-extension-research-associate-2-korean-chinese-or-spanish-bilingual-riverside-ca-job-id-85196</guid>
								<description>Riverside, California,  Small Farms Extension &#38; Research Associate 2 (Korean, Chinese, or Spanish Bilingual)  Riverside, CA, Job ID 85196 University of California Agriculture and Natural Resources Job Description      Position Summary: The Small Farms Extension and Research Associate will assist UC ANR Small Farms Advisors in the delivery of technical assistance, training, outreach, and applied research activities to increase extension support for small-scale, diversified, and historically underserved farmers. Areas of focus include on-farm production challenges such as irrigation, nutrient management, and pest management; regulatory compliance; marketing and business support; and incentive program and grant application technical support. Working under the general direction of a county-based Small Farms Advisor, the Associate assists UC ANR academics, staff, and collaborating growers with collection and analysis of data needed for grower surveys, applied research projects, program development and evaluation, and policy communications. The Associate will also provide expert, technical assistance in English, as well as Korean, Chinese, or Spanish to small-scale farmers to enhance on-farm productivity, compliance with local, state, and federal regulatory programs, and access to resources such as grants, incentives programs, and emergency relief programs. The Associate will assist UC ANR academics in the extension of applied research results and the development, delivery, and evaluation of bilingual, culturally appropriate, research-based educational materials and extension programming to support small-scale, diversified, and historically underserved farmers. The Associate will develop and conduct effective methods to increase outreach and participate in program evaluation, needs assessments, and strategic planning for outreach and extension efforts in the assigned county or counties. Applied research duties include assisting with survey development and translation, recruitment of farmer participants, setup of field experiments, data collection and management, basic data analysis for outreach, educational programming, and research projects. Research, outreach, and extension efforts will also be coordinated with a statewide network of Small Farms Advisors and program staff in multiple counties. The Small Farms Network will work closely with partner agencies and non-profit organizations to coordinate and leverage statewide technical assistance efforts. The position requires regular travel to farms within assigned counties, including remote and rural areas, a minimum of two days per week as needed, and occasional travel outside the assigned counties. This position will cover Riverside and San Bernardino Counties. This position is a career appointment that is 100% fixed.  Pay Scale:  $31.23 /hour to $39.60/hour Job Posting Close Date:  This job is open until filled. The first application review date will be 04/15/2026. Key Responsibilities: 75%    Provide growers with direct, one-on-one, bilingual technical assistance and extension support. Travel to farms, conduct farm visits and meet with farmers individually to assist with production challenges, marketing, regulatory compliance, and access to grants, incentives, and economic relief programs. Assist farmers with online applications and collect data to identify barriers to access to programs.    Assist with survey development and data collection for county-level and statewide needs assessments to inform strategic planning of outreach, training, and applied research efforts. Assist with translation and review of survey questions. Assist with recruitment of survey participants.    Collect and organize evaluation data from participants at workshops and individual farm visits. Gather input from farmers and conduct basic analyses of data to inform program improvements.    Organize and maintain electronic records such as farmer contact lists and coordinate bilingual outreach through radio, social media, newsletters, farm visits, and networking. Organize, promote, and assist with extension workshops on a range of research, extension, and technical assistance topics.    Gather data to inform policy discussions, including feedback from partner organizations, and summarize results for policy communications. Develop and deliver presentations at meetings with nonprofit partner organizations, regulatory agencies, and policy makers to provide research-based information on the needs and challenges of small-scale farms and to develop new collaborations.    Develop and design bilingual educational materials and deliver educational programming to assist small-scale farmers in accessing markets and assistance programs, complying with regulations in areas such as food safety, labor, groundwater use, fertilizer use, pesticide use, and organic certification, and addressing crop production challenges through improved irrigation, nutrient management, pest management, and other production practices.    Serve as a lead worker on multi-county outreach and technical assistance efforts where background and expertise are sufficient to serve as a subject matter expert for specific project topics.    Collect soil, plant, insect, water, and other types of samples to assist with research and technical support activities. 15%    Assist the Small Farms Advisor with research activities and data management, including data collection for field research trials. Travel to field research sites to complete activities.    Keep accurate and timely records and develop systems to organize reporting data. Manage database and Excel records, assist with tracking of activities, farmer contacts, and expenses, organize information for program evaluation, and prepare data summaries.    Conduct basic data analysis on demographic, survey, and field trial data.    Provide oral and written reports on a regular basis on data collection and results.    Assist in development of reports as required by funding agencies and internal reporting procedures. 10%    Provide coordination and bilingual support for outreach projects with growers, such as on-farm demonstrations and tailgate meetings.    Order supplies for research and extension projects.    Prepare equipment and supplies necessary for field work and data collection.    Recruit farmers to participate in on-farm research trials and assist with translation and communication to facilitate research activities.    Coordinate logistics necessary for data collection with county office staff and other research assistants.    Keep academics, staff, and other project collaborators informed of data collection status, pertinent results, and issues affecting research projects.    Travel to farms to conduct outreach, training, and research activities. Requirements: A minimum of a Bachelor&#39;s degree with coursework in the agricultural or social sciences relevant to agricultural extension, applied research, and community engagement and/or equivalent experience or training. Excellent organizational skills to collect data and maintain integrity of data.  Ability to pay attention to details and produce accurate results.  Proficiency in Microsoft Office applications including Word, Excel, and PowerPoint.  Excellent time management skills and the ability to manage multiple project tasks to ensure successful completion. Excellent verbal and written communication and interpersonal skills to communicate complex agronomic, business, and regulatory topics to in a manner understandable to growers. Ability to analyze, evaluate and synthesize information relevant to grower needs and challenges, applications of research results, and policy communications. Experience working in an agricultural setting or directly working with farmers.  Proficient bilingual communication skills including the ability to read, write, translate, and effectively communicate technical agricultural information in a language relevant to growers within the county region served by the position, such as Spanish, Hmong, Chinese, or Korean. This position requires bilingual communication skills in English and Korean, Chinese, or Spanish. Preferred Skills: General knowledge of the biological and natural sciences, including fields such as soils, entomology, and plant physiology and pathology, and/or general knowledge of the social and economic sciences. Working knowledge of basic agricultural research methods and/or experience in applied research.  Experience conducting surveys, focus groups, analysis of demographic data, or other social science research methods. Experience in extension, adult education, project coordination, public speaking, community development, or community outreach. Demonstrated skills and experience communicating research results to diverse audiences.  Experience working with disadvantaged, marginalized, or historically underserved communities. Special Conditions of Employment: Must possess valid California Driver&#39;s License to drive a County or University vehicle. Ability and means to travel on a flexible schedule as needed, proof of liability damage insurance on vehicle used is required. Reimbursement of job-related travel will be reimbursed according to University policies. Ability and means to travel to farms within assigned counties, including remote and rural areas, a minimum of two days per week as needed, and occasional travel outside the assigned counties. Travel including travel outside normal business hours may be requested. Overtime and occasional weekend work as needed, usually on short notice to meet operational needs may be requested. The University reserves the right to make employment contingent upon successful completion of the background check. This is a designated position requiring a background check and may require fingerprinting due to the nature of the job responsibilities. UC ANR does hire people with conviction histories and reviews information received in the context of the job responsibilities. As of January 1, 2014, ANR is a smoke- and tobacco-free environment in which smoking, the use of smokeless tobacco products, and the use of unregulated nicotine products (e-cigarettes), is strictly prohibited. As a condition of employment, you will be required to comply with the University of California  https://apptrkr.com/get_redirect.php?id=7038737&#38;targetURL= Policy on Vaccination Programs , as may be amended or revised from time to time.  Federal, state, or local public health directives may impose additional requirements. Misconduct Disclosure Requirement:   As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer.  a. &#39;Misconduct&#39; means any violation of the policies or laws governing conduct at the applicant&#39;s previous place of employment, including, but not limited to, violations of policies or laws prohibiting sexual harassment, sexual assault, or other forms of harassment, discrimination, dishonesty, or unethical conduct, as defined by the employer.  For reference, below are UC&#39;s policies addressing some forms of misconduct:  UC Sexual Violence and Sexual Harassment Policy  UC Anti-Discrimination Policy   Abusive Conduct in the Workplace      To apply, please visit:  https://careerspub.universityofcalifornia.edu/psc/ucanr/EMPLOYEE/HRMS/c/HRS_HRAM_FL.HRS_CG_SEARCH_FL.GBL?Page=HRS_APP_JBPST_FL&#38;JobOpeningId=85196&#38;PostingSeq=1&#38;SiteId=17&#38;languageCd=ENG&#38;FOCUS=Applicant Copyright 2025 Jobelephant.com Inc. All rights reserved. Posted by the FREE value-added recruitment advertising agency   jeid-ad54e0115200af4b8b86c94317b6e983</description>
								<pubDate>Fri, 24 Apr 2026 02:26:20 -0400</pubDate>
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									<link>https://careers.chpa.org/jobs/rss/22047261/leo-lecturer-iii-college-of-innovation-technology-smart-manufacturing-onsite</link>
								
								<title>LEO Lecturer III - College of Innovation &#38; Technology - Smart Manufacturing - Onsite | University of Michigan - Flint</title>								
								<guid isPermaLink="true">https://careers.chpa.org/jobs/rss/22047261/leo-lecturer-iii-college-of-innovation-technology-smart-manufacturing-onsite</guid>
								<description>Flint, Michigan,  ATTENTION: FACULTY APPLICANTS APPLY HERE  ( https://apply.interfolio.com/181196 ) to view the position details and submit your application materials. The University of Michigan-Flint currently utilizes Interfolio for all faculty positions. DO NOT USE THE APPLY NOW BUTTON AT THE TOP OF THIS PAGE.  If you are interested in applying for this position with (insert department, college and/or school), please use the Interfolio link provided ( https://apply.interfolio.com/181196 ).&#xa0; Applications submitted through this page, may not be considered for this position. For further information and/or assistance, please contact Ally Cooper, Administrative Assistant at callyso@umich.edu. The University of Michigan is an equal employment opportunity employer. &#xa0;</description>
								<pubDate>Fri, 24 Apr 2026 00:27:44 -0400</pubDate>
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									<link>https://careers.chpa.org/jobs/rss/22184109/retail-pharmacy-technician</link>
								
								<title>Retail Pharmacy Technician | WMCHealth</title>								
								<guid isPermaLink="true">https://careers.chpa.org/jobs/rss/22184109/retail-pharmacy-technician</guid>
								<description>Valhalla, New York,  Job Summary :  The Retail Pharmacy Technician supports the pharmacy team by assisting in the preparation, dispensing, and management of medications while ensuring compliance with all regulatory requirements. This role focuses on delivering exceptional customer service, maintaining accurate records, and promoting patient safety. &#xa0; &#xa0; Responsibilities: Prescription Processing: Receive and verify prescription orders for accuracy and completeness. Enter prescription information into the pharmacy system. Prepare and label medications under the supervision of a licensed pharmacist. Customer Service: Greet and assist customers in a professional and courteous manner. Answer questions regarding prescriptions, refills, and general pharmacy inquiries. Handle transactions, including insurance claims and payment processing. Inventory Management: Maintain stock levels and organize medication storage areas. Assist in ordering, receiving, and checking inventory for accuracy. Monitor expiration dates and remove outdated medications. Compliance &#38; Safety: Adhere to state and federal pharmacy regulations. Maintain confidentiality of patient information (HIPAA compliance). Follow proper procedures for controlled substances. &#xa0; Qualifications/Requirements: Experience:  Minimum of 1&#8211;2 years  working in a retail pharmacy or similar healthcare setting preferred. &#xa0; Education:  High school diploma or equivalent required.  Completion of an accredited Pharmacy Technician training program preferred.   &#xa0; Licenses / Certifications:   Current NYS pharmacist license required, or eligible to obtain within 90 days of hire. Other:  Reports to Retail Pharmacist   &#xa0;</description>
								<pubDate>Fri, 24 Apr 2026 00:58:53 -0400</pubDate>
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									<link>https://careers.chpa.org/jobs/rss/22156682/clinical-research-assistant-psychiatry</link>
								
								<title>Clinical Research Assistant - Psychiatry | The Ohio State University</title>								
								<guid isPermaLink="true">https://careers.chpa.org/jobs/rss/22156682/clinical-research-assistant-psychiatry</guid>
								<description>,  Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the Weafer Alcohol Research Laboratory in the Department of Psychiatry and Behavioral Health. We are an advanced cognitive neuroscience research lab studying alcohol use, with a focus on sex differences and risk factors for women. We utilize functional magnetic resonance imaging (fMRI), hormonal assays, and intravenous alcohol administration to study the neural, behavioral, and hormonal factors underlying risk for alcohol use disorder. We are looking to recruit a highly skilled, organized, responsible, motivated, and conscientious individual to manage NIAAA-funded research projects focused on sex differences in risk for alcohol use disorder. The Clinical Research Coordinator assists with screening and identifying volunteers who are eligible to participate in specified clinical research protocols; recruits, interviews and enrolls participants; obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements; educates participants of purpose, goals, and processes of clinical study; coordinates scheduling and follow-through of study appointments and procedures in accordance with study protocol; participates in the collection, processing  administers, evaluates and calculates standardized scoring of diagnostic, psychological and behavioral testing and questionnaires; assists with monitoring participants for adverse reactions to study drug or procedure and notifies appropriate clinical professional to evaluate participant response, identify status of complications,  documents unfavorable responses and notifies research sponsors  participates in evaluating participants for compliance related to protocol; assists with collecting, extracting, coding, and analyzing clinical research data; generates reports and reviews to ensure validity of data; supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations; assists with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors; participates in activities to develop new research protocols and contributes to establishment of study goals to meet protocol requirements.  Minimum Education and Skills/Experience Required/Desired Bachelors Degree in biological sciences, health sciences, social sciences or other medical field or an equivalent combination of education and experience required; one year experience in a clinical research capacity required; experience or knowledge in alcohol research preferred; knowledge of medical terminology desired; clinical research certification from an accredited certifying agency desired; computer skills required with experience using Microsoft Software applications desired. Requires successful completion of a background check. Qualified candidates may be requested to complete a pre-employment physical, including a drug screen. Function: Research and Scholarship Sub-function: Clinical Research Career Level: S2</description>
								<pubDate>Fri, 24 Apr 2026 02:33:33 -0400</pubDate>
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									<link>https://careers.chpa.org/jobs/rss/22027845/assistant-director-for-research-national-center-for-the-elimination-of-educational-disparities</link>
								
								<title>Assistant Director for Research, National Center for the Elimination of Educational Disparities | Morgan State University</title>								
								<guid isPermaLink="true">https://careers.chpa.org/jobs/rss/22027845/assistant-director-for-research-national-center-for-the-elimination-of-educational-disparities</guid>
								<description>Baltimore, Maryland,  Duties &#38; Responsibilities: Lead a team of faculty in the development of a research agenda and in the design and implementation of research-based interventions aimed at removing barriers to equitable outcomes for P-12 learners in the State of Maryland and beyond. In addition to implementing the state-supported research of NCEED, the Assistant Director will also be expected to seek external funding in support of the work of the Center. Research Leadership &#38; Management ? Provide oversight for research projects from inception to completion, including design, methodology, implementation, and reporting. ? Support faculty in the dissemination of research findings in scholarly, practitioner, and community venues. ? Supervise and mentor post-doctoral fellows, graduate assistants, and undergraduate research fellows ? Support the Director in fulfilling the Center?s research agenda and strategic priorities. ? Work collaboratively with other units within the university during the pre-award and post-award phases to ensure compliance with regulatory requirements. Monitor progress across multiple projects to ensure methodological rigor, timely delivery and compliance with ethical standards for research, and alignment with institutional and state compliance goals. Assist the Director by maintaining an inventory of all grant, contract, and inter-agency activities. ? Prepare reports on the status of all grants, contracts, and inter-agency activities for the Director Grant Development &#38; Funding ? Identify funding opportunities from federal, state, and philanthropic organizations and foundations, and assist with the preparation of competitive grant proposals from project conceptualization to submission. ? Coordinate pre-award budget development and post-award financial management for funded projects. ? Ensure compliance with sponsor guidelines, reporting requirements, and institutional and state policies. ? Post-award, ensure that research goals and objectives are accomplished on time, and within budgetary constraints in accordance with the grant as approved. Partnerships &#38; Collaboration ? Build and maintain strong relationships with K-12 schools, local educational agencies, higher education institutions, and philanthropic networks ? Foster collaborations with faculty, research partners, government agencies, and community organizations. ? Represent the Center in academic, professional, and policy forums as well as education-focused community events ? Support the development of partnerships within the School of Education and Urban Studies, as well as interdisciplinary initiatives and cross-institutional partnerships. ? Support the work of research-practice partnerships in the generation of research that could inform practice. Knowledge Dissemination ? Oversee the preparation of research outputs, including reports, peer-reviewed publications, policy briefs, and presentations. ? Develop strategies for research translation and knowledge mobilization to reach diverse audiences. ? Organize conferences, workshops, and seminars to be hosted by the Center. Administrative &#38; Strategic Support ? Assist the Director in long-term planning, resource allocation, and evaluation of research impact. Manage compliance with ethical standards, IRB protocols, and data management requirements, and alignment with institutional strategic goals</description>
								<pubDate>Fri, 24 Apr 2026 00:27:40 -0400</pubDate>
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									<link>https://careers.chpa.org/jobs/rss/22195164/physical-therapist-assistant-prn-weekends</link>
								
								<title>Physical Therapist Assistant - PRN - Weekends | Northeast Georgia Health System</title>								
								<guid isPermaLink="true">https://careers.chpa.org/jobs/rss/22195164/physical-therapist-assistant-prn-weekends</guid>
								<description>Gainesville, Georgia,  Job Category: Allied Health Work Shift/Schedule: 8 Hr Morning - Afternoon Northeast Georgia Health System is rooted in a foundation of improving the health of our communities.   About the Role: Job Summary Provides physical therapy treatments as designed by the supervising physical  therapist. Provides  ongoing care independently, consulting with the Physical Therapist regarding changes in treatment and  discharge. Provides  care/service that meets the developmental needs of patients across the life span as appropriate to the patient population and as indicated on the skills checklist. This position will care for patients in the child, adolescent, adult, and geriatric age  groups. Employee  performs clinical duties in accordance with population specific guidelines and adheres to National Patient Safety Goals as outlined in policy and procedures.   Minimum Job Qualifications Licensure or other certifications:  Current license holder of the Georgia Board of Physical Therapy. Educational Requirements:  Associates Degree. Graduate of an approved school of Physical Therapy, Assistant. Minimum Experience:  One (1) year of experience as Physical Therapy Assistant. New graduates from approved school for Physical Therapy Assistants will be considered. Other: Preferred Job Qualifications Preferred Licensure or other certifications: Preferred Educational Requirements:  Preferred Experience: Other: Job Specific and Unique Knowledge, Skills and Abilities Has skills as determined by accredited educational institutes requirements to provide patient care that meets developmental needs across the life span Must know correct body mechanics and lifting techniques Essential Tasks and Responsibilities Conducts physical therapy according to the physical therapy plan of care.  Provides quality rehabilitative care to patients as outlined in the treatment plan. Completes all required documentation according to regulatory agency and departmental standards. Notifies appropriate therapist of the patient&#39;s progress and suggests changes in the plan of care when indicated. Assists in discharge planning by assuring the patient has appropriate equipment at home, and family is aware of a home exercise program. Performance monitored by feedback from discharge planners and physical therapist. Ensures re-evaluation of the patient and plan of care is completed by the therapist as indicated. Contributes to the effective operation of the department and consistently meets or exceeds the program productivity standards.  Asks for assistance from other staff when necessary for patient care and  safety. Delegates  appropriately to techs and works within the Georgia state practice act for physical therapy, and according to the code of ethics established by the APTA. Accepts work in other programs as requested by management. Communicates effectively and demonstrates good interpersonal skills and professionalism. Finishes all job assignments in a timely manner as determined by direct supervisor.  Physical Demands Weight Lifted:  Up to 50 lbs, Frequently 31-65% of time Weight Carried:  Up to 20 lbs, Frequently 31-65% of time Vision:  Moderate, Frequently 31-65% of time Kneeling/Stooping/Bending:   Frequently 31-65% Standing/Walking:  Frequently 31-65% Pushing/Pulling:  Frequently 31-65% Intensity of Work:  Frequently 31-65% Job Requires:   Reading, Writing, Reasoning, Talking, Keyboarding Working at NGHS means being part of something special: a team invested in you as a person, an employee, and in helping you reach your goals.  NGHS: Opportunities start here. Northeast Georgia Health System is an Equal Opportunity Employer and will not tolerate discrimination in employment on the basis of race, color, age, sex, sexual orientation, gender identity or expression, religion, disability, ethnicity, national origin, marital status, protected veteran status, genetic information, or any other legally protected classification or status.</description>
								<pubDate>Fri, 24 Apr 2026 00:42:42 -0400</pubDate>
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									<link>https://careers.chpa.org/jobs/rss/22132626/clinical-research-coordinator-i</link>
								
								<title>CLINICAL RESEARCH COORDINATOR I | University of Alabama, Birmingham</title>								
								<guid isPermaLink="true">https://careers.chpa.org/jobs/rss/22132626/clinical-research-coordinator-i</guid>
								<description>Birmingham, Alabama,  Job Description The University of Alabama at Birmingham (UAB), Ped - Neonatology, is seeking a Clinical Research Coordinator I. The Clinical Research Coordinator I (CRC I) will support the Healthy Brain and Child Development (HBCD) Study, the largest U.S. long-term study on early brain and child development. This multi-site study follows pregnant individuals and their infants through childhood to explore early brain development. The CRC I will assist with recruitment, scheduling, participant visits, data collection, and study coordination. This position requires quick learning of study procedures, including MRI, EEG, biosample collection, and data management systems (e.g., Ripple and LOR).   General Responsibilities   To serve as coordinator for studies and provide support to other team members within the confines of the protocol as directed. To support screening and participant eligibility determination, working with more senior team members to ensure compliance. To conduct activities in accordance with the protocol, regulations and Good Clinical Practice (GCP). To assist with the study life cycle from start-up to closure, i.e., collecting and recording data, recruiting and performing follow-up with participants, scheduling visits and assisting in coordination of lab and fieldwork.   Key Duties &#38; Responsibilities   Conducts study visits involving MRI, EEG, behavioral assessments, biosensors, and specimen collection (blood, urine, stool, saliva, nails). Follows SOPs for data collection and equipment usage; trains others as needed. Ensures timely and accurate data entry in systems such as Ripple and LORIS, and assists in monitoring data quality. Leads and supports recruitment efforts focused on second-trimester individuals from diverse backgrounds. Collaborates with Study Navigators to organize recruitment schedules and develop referral relationships. Implements outreach strategies to support participant enrollment and retention over a 10-year longitudinal study. Leverages knowledge of Alabama health systems and resources to support participant families. Conducts and documents informed consent procedures. Maintains comprehensive participant records, visit schedules, and recruitment tracking tools. Monitors recruitment and retention metrics, proposing solutions for identified challenges. Trains and mentors junior staff and students in study protocols, data collection procedures, and ethical research practices. Oversees daily task assignments and monitors completion of responsibilities. Collects, processes, and ships biospecimens following study protocols. Maintains accurate biospecimen documentation to ensure chain of custody and regulatory compliance. Contributes to updates and refinements of SOPs and operational processes. Assists in IRB submissions and protocol documentation. Coordinates with financial staff on budgeting, participant payments, and supply orders. Ensures accurate use of electronic data systems and technology platforms. Performs other duties as assigned.   Annual Salary Range :     $43,890 - $71,320 Qualifications High School diploma or GED required.   UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran&#39;s status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UAB&#39;s Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix. Job:Clinical Research</description>
								<pubDate>Fri, 24 Apr 2026 00:47:04 -0400</pubDate>
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									<link>https://careers.chpa.org/jobs/rss/22193715/clinical-research-coordinator-neurology</link>
								
								<title>Clinical Research Coordinator - Neurology | The Ohio State University</title>								
								<guid isPermaLink="true">https://careers.chpa.org/jobs/rss/22193715/clinical-research-coordinator-neurology</guid>
								<description>,  Job Description Summary Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the College of Medicine (COM) Center for Clinical Research Management (CCRM) the Department of Neurology/ Division of Neuromuscular Diseases, with a focus on  Amyotrophic Lateral Sclerosis   (ALS), or Lou Gehrig&#39;s disease ; assists with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols; recruits, interviews and enrolls patients; obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements; educates patients and families of purpose, goals, and processes of clinical study; coordinates scheduling and follow-through of patient care appointments, procedures,  participates in the collection, processing  administers, evaluates and calculates standardized scoring of diagnostic, psychological or behavioral testing or questionnaires; assists with monitoring patients for adverse reactions to study treatment, procedure or medication and notifies appropriate clinical professional to evaluate patient response, identify status of complications,  documents unfavorable responses and notifies research sponsors  participates in evaluating patients for compliance related to protocol; assists with collecting, extracting, coding, and analyzing clinical research data; generates reports and reviews to ensure validity of data; supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations; assists with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors; participates in activities to develop new research protocols and contributes to establishment of study goals to meet protocol requirements.  Minimum Education Required Bachelors Degree in biological sciences, health sciences, social sciences or other medical field or an equivalent combination of education and experience required. Required Experience One year experience in a clinical research capacity required. Preferred Experience Experience or knowledge in cognitive diseases/disorders preferred. Desired Qualifications Knowledge of medical terminology desired; clinical research certification from an accredited certifying agency desired; computer skills required with experience using Microsoft Software applications desired. Requires successful completion of a background check. Qualified candidates may be requested to complete a pre-employment physical, including a drug screen. FUNCTION/SUBFUNCTION: Research and Scholarship/Clinical Research CAREER BAND: Individual Contributor-Specialized CAREER LEVEL: S2   This position is patient facing and is required to be onsite. Travel to other Ohio State Wexner Medical Center outpatient locations such as Outpatient Care East, Dublin, and New Albany may be required.</description>
								<pubDate>Fri, 24 Apr 2026 02:33:33 -0400</pubDate>
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									<link>https://careers.chpa.org/jobs/rss/22165843/clinical-research-coordinator-hs-neurological-surgery</link>
								
								<title>Clinical Research Coordinator (HS)- Neurological Surgery | The Ohio State University</title>								
								<guid isPermaLink="true">https://careers.chpa.org/jobs/rss/22165843/clinical-research-coordinator-hs-neurological-surgery</guid>
								<description>,  Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer College of Medicine (COM) Center for Clinical Research Management (CCRM) for the Department of Neurological Surgery Human Gene Therapy Clinical Research Team; assists with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols; recruits, interviews and enrolls patients; obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements; educates patients and families of purpose, goals, and processes of clinical study; coordinates scheduling and follow-through of patient care appointments, procedures,  participates in the collection, processing  administers, evaluates and calculates standardized scoring of diagnostic, psychological or behavioral testing or questionnaires; assists with monitoring patients for adverse reactions to study treatment, procedure or medication and notifies appropriate clinical professional to evaluate patient response, identify status of complications,  documents unfavorable responses and notifies research sponsors  participates in evaluating patients for compliance related to protocol; assists with collecting, extracting, coding, and analyzing clinical research data; generates reports and reviews to ensure validity of data; supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations; assists with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors; participates in activities to develop new research protocols and contributes to establishment of study goals to meet protocol requirements. Minimum Education Required Bachelors Degree in biological sciences, health sciences, social sciences or other medical field or an equivalent combination of education and experience required. Required Experience One year experience in a clinical research capacity required. Experience and Skills Preferred Experience or knowledge in inpatient clinical research preferred; knowledge of medical terminology desired; clinical research certification from an accredited certifying agency desired; computer skills required with experience using Microsoft Software applications desired. Requires successful completion of a background check. Qualified candidates may be requested to complete a pre-employment physical, including a drug screen. FUNCTION/SUBFUNCTION: Research and Scholarship/Clinical Research CAREER BAND: Individual Contributor- Specialized CAREER LEVEL: S2   This position is patient facing and is required to be onsite at The Ohio State University Wexner Medical Center. Evenings, weekends, holidays, and on-call hours may be required as dictated by the clinical research activity.</description>
								<pubDate>Fri, 24 Apr 2026 02:33:33 -0400</pubDate>
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									<link>https://careers.chpa.org/jobs/rss/22046437/clinical-research-coordinator-float-clinical-trials-management-office</link>
								
								<title>Clinical Research Coordinator Float-Clinical Trials Management Office | The Ohio State University</title>								
								<guid isPermaLink="true">https://careers.chpa.org/jobs/rss/22046437/clinical-research-coordinator-float-clinical-trials-management-office</guid>
								<description>,  Clinical Research Coordinator- Float to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the College of Medicine (COM) Center for Clinical Research Management (CCRM) in various COM Departments and Divisions conducting non-oncology human subjects research; assists with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols; recruits, interviews and enrolls patients; obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements; educates patients and families of purpose, goals, and processes of clinical study; coordinates scheduling and follow-through of patient care appointments, procedures,  participates in the collection, processing  administers, evaluates and calculates standardized scoring of diagnostic, psychological or behavioral testing or questionnaires ;  assists with monitoring patients for adverse reactions to study treatment, procedure or medication and notifies appropriate clinical professional to evaluate patient response, identify status of complications,  documents unfavorable responses and notifies research sponsors  participates in evaluating patients for compliance related to protocol; assists with collecting, extracting, coding, and analyzing clinical research data; generates reports and reviews to ensure validity of data; supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations; assists with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors; participates in activities to develop new research protocols and contributes to establishment of study goals to meet protocol requirements.  Minimum Education Required Bachelors Degree in biological sciences, health sciences, social sciences or other medical field or an equivalent combination of education and experience required. Minimum Experience Required One year experience in a clinical research capacity required. Computer experience required. Experience Preferred Experience or knowledge in   coordinating clinical trials  preferred; knowledge of medical terminology desired; clinical research certification from an accredited certifying agency desired. Experience using Microsoft applications desired and knowledge of data base systems such as RedCap, Medidata, Rave, etc. Requires successful completion of a background check. Qualified candidates may be requested to complete a pre-employment physical, including a drug screen. FUNCTION/SUBFUNCTION: Research and Scholarship/Clinical Research CAREER BAND: Individual Contributor-Specialized CAREER LEVEL: S2   This position is patient facing and is required to be on site. Travel to various clinical research locations will be required. Locations may include Outpatient Care East, Outpatient Care New Albany, Outpatient Care Dublin, Martha Morehouse, Upper Arlington, etc.</description>
								<pubDate>Fri, 24 Apr 2026 02:33:33 -0400</pubDate>
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