Responsible for all data management aspects of clinical studies and efficiently performs all data management activities within an assigned study or studies.
Provide data management expertise to the team in identifying opportunities for improvement.
Ensure validity of research results through timely, accurate, and complete data submission, query resolution, and reporting of deviations.
Demonstrate proficiency in the use of clinical and research-related computer programs.
Research Conduct/Study Management:
Ensure that relevant data from the source document are abstracted and recorded in the clinical trial case report forms and that every data point can be verified within the source document.
Utilize analytical thinking, attention to detail, and problem-solving skillsÂ
Regulatory Compliance and Other:
Facilitate communication between the site and study sponsor, CRO, and/or regulators and exhibits teamwork skills necessary for managing the data collection and reporting process.
May assist in training other Data Managers within the unit.
Prepares for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
Participates in study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
Performs other related work as needed.
One year of research experience or relevant experience
Demonstrated ability to abstract subject data from medical record/source documentation and enter into care report forms and/or databases.
Experience generating and resolving queries and/or monitoring data.
Ability to handle competing demands with diplomacy and enthusiasm.
Ability to perform research data management with minimal supervision.
Strong data management skills and attention to detail.
Ability to work collaboratively and with divisional research offices.
Knowledge of Microsoft Word, Excel and Adobe Acrobat.
Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data.
Adaptability to changing working situations and work assignments.
Ability to work independently and as part of a team.
Strong attention to detail.
Excellent multi-tasking skills.
Knowledge of medical and/or /clinical trial terminology.
Knowledge in relevant scientific field.
Ability to train junior data managers.
Cover Letter (required)
The University of Chicago is an Affirmative Action/Equal Opportunity/Disabled/Veterans Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national or ethnic origin, age, status as an individual with a disability, protected veteran status, genetic information, or other protected classes under the law. For additional information please see the University's Notice of Nondiscrimination.
Staff Job seekers in need of a reasonable accommodation to complete the application process should call 773-702-5800 or submit a request via the Applicant Inquiry Form.
The University of Chicago's Annual Security & Fire Safety Report (Report) provides information about University offices and programs that provide safety support, crime and fire statistics, emergency response and communications plans, and other policies and information. The Report can be accessed online at: securityreport.uchicago.edu. Paper copies of the Report are available, upon request, from the University of Chicago Police Department, 850 E. 61st Street, Chicago, IL 60637.
Internal Number: JR09163
About University of Chicago (UC)
One of the world's premier academic and research institutions, the University of Chicago has driven new ways of thinking since our 1890 founding. Today, UChicago is an intellectual destination that draws inspired scholars to our Hyde Park and international campuses, keeping UChicago at the nexus of ideas that challenge and change the world.