This position may independently provide study coordination for simple and moderately complex clinical research studies.As a member of a coordination team, this position may help support a portfolio of projects with varying levels of complexity.Mastery of all job duties from the Clinical Research Assistant position is required.
Clinical coordinator-After completion of team training, learns to consent and enroll patients into observational studies and clinical trials.Performs study visits including pre-visit preparation, data and biosample collection during visits, shipping of materials and data entry.Arranges follow-up protocol study visits.Interfaces with data coordinating site and monitors.
Data coordinator-Works to address data queries, site monitoring visits, conference calls, data entry into web based systems
Regulatory-submission and management of IRB applications, ORIO?s, and adverse events.Assist with completing new e-research applications ; maintaining reg binders.Interfacing with sponsors.
Administrative- Collection and processing of biosamples and data, data entry, scheduling patients.Assisting with recruitment efforts with internal and external medical providers.Obtaining outside records and tissue samples.
Characteristic Duties and Responsibilities: Expert level knowledge, skills, and abilities within all 8 competency domains is expected:
Scientific Concepts and Research Design
Ethical Participant Safety Considerations
Investigational Products Development and Regulation
Clinical Study Operations (GCPs)
Study and Site Management
Data Management and Informatics
Leadership and Professionalism
Communication and Teamwork
Supervision Received: This position reports directly to a faculty PI
Supervision Exercised: None
Associate degree in Health Science or an equivalent combination of related education and experience is necessary.
Minimum 1 year of directly related experience in clinical research and clinical trials is necessary. (Please review SoCRAs Definition of a Clinical Research Professionalfor qualifying experience prior to applying.) or An advanced degree in a health-related areas such as: Health Sciences, Behavioral Sciences, Public Health, Health Care Administration, Clinical Research Administration, Social Work, Psychology, Epidemiology, Foreign MD. or Minimum 3 years of human subject experience (clinical, lab or health regulations) such as related patient care, related community health and wellness, related clinical information, and research.
Anunderstanding of medical terminology, experience in a large complex health care setting, ability to effectively communicate with staff and faculty of all levels, and knowledge of university policies and procedures is desirable.
Minimum of 1 year of prior experience in human subjects research.
M-F normal business hours and onsite
Michigan Medicine is firmly committed to advancing inclusion, diversity, equity, accessibility, and belonging, which are core to the culture and values of the Medical School Office of Research. Our community supports recruiting and cultivating a diverse workforce as a reflection of our commitment to serve the diverse people of Michigan and the world. We strive to create a work culture where each team member feels respected, valued, and safe.
Michigan Medicine conducts background screening and pre-employment drug testing on job candidates upon acceptance of a contingent job offer and may use a third party administrator to conduct background screenings. Background screenings are performed in compliance with the Fair Credit Report Act. Pre-employment drug testing applies to all selected candidates, including new or additional faculty and staff appointments, as well as transfers from other U-M campuses.
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