1) Regulatory Affairs Managers function as essential members of our dynamic clinical research teams by managing regulatory functions for studies conducted in the Department of Medicine.Â
2) These clinical research studies may involve various areas of medicine and modalities of treatment.
3) Research projects include investigator authored studies, as well as industry sponsored research.Â
4) Regulatory Affairs Managers handle all regulatory functions for a large portfolio of studies.Â
5) This includes Institutional Review Board (IRB) approval, all specialty subcommittee reviews, and FDA IND and IDE submission.Â
6) Regulatory Managers serve as liaisons between principle investigator, co-investigators, sponsoring agents, regulatory agencies, and other members of the research team.
7) Regulatory Managers lead PIâ™s and study teams in meeting internal and external regulatory compliance requirements, and serve a vital role during study audits.
8) Partner with PI study team to maximize clinical research efficiency and progress.
9) Consult with PI team regarding strategic planning around clinical research portfolios.
10) Participate in protocol writing.
11) Facilitate study initiation through thoughtful and timely preparation of IRB, sub-committee and FDA submissions.
12) Prepare and maintain all materials related to IRB and FDA approvals.
13) Ensure successful monitoring and auditing of studies including FDA, sponsor and/or internal study audits.
14 )Present research portfolio progress during research team meetings.
15) Provide guidance to faculty regarding compliance, funding and research support resources.
16) Maintain a high level of self-education to include review of articles related to clinical research; attend multi-disciplinary conferences; attend workshops specific to clinical research.
17) Assist in the orientation and training of new and current Clinical Research Support Office staff and/or staff in the various sections of the Department of Medicine. Â
1) Outstanding project management.
2) Excellent verbal and written communication skills.
3) Ability to manage stressful situations.
4) Analytical thinking and problem-solving.
5) Attention to detail.
6) Strong organizational skills.
7) Strong Interpersonal skills.
8) Work independently with a high degree of initiative.
9) Work as part of a team.
10) Ability to maintain confidentiality.
11) Proficiency with Microsoft Word and Excel.
12) Proficiency with Adobe Acrobat.
1) Bachelor's degree
1) 1-2 years of project management experience
2) Regulatory compliance experience
3) Clinical research and/or data management experience
4) Experience at a large academic or medical institution
2) Cover letter
Note: When applying, all required documents MUST be uploaded under the Resume/CV section of the application.
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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.
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About University of Chicago
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