Clinical Research Manager, Research Incubation Unit
University of ChicagoAbout the role
Department
BSD OCR - Clinical Research Operations
About the Department
The mission of the Office of Clinical Research is to catalyze clinical research by providing expertise, resources, infrastructure, and systems that facilitate clinical research operations and enable collaboration across the enterprise while promoting compliance and human subject protection on behalf of our diverse community of patients and volunteers. Together, we elevate the human experience with knowledge and health care.
Job Summary
The Clinical Research Manager manages a team of professional staff responsible for clinical research conduct , research participant management, data management, and regulatory. Key responsibilities of the Manager include recruiting, onboarding, and training of new clinical research staff; day-to-day management and supervision of clinical research staff; supporting study initiation and completion of key milestones throughout the life cycle of the trials; tracking and reporting on key metrics; communicating with investigators and department leaders; communicating with industry sponsors and internal stakeholders; and fulfilling service level agreement performance standards. This position will have primary accountability to the Director of Clinical Research Operations within the Office of Clinical Research.
Responsibilities
Oversee Departmental Clinical Research Portfolio across the lifecycle for each protocol from feasibility, startup, recruitment, day-to-day conduct, follow up through study close out.
Coordinate departmental clinical research staff and faculty meetings.
Oversee the conduct of clinical research, regulatory compliance, and IRB filings for all projects in the departmental portfolio.
Establish documentation standards for departmental scientific review and feasibility for all proposed clinical research projects.
Establish departmental standard work and standard operating procedures.
Monthly Reports of site performance and percent effort reports.
Training and onboarding of all research staff in GCP, 21 CFR 11, 21 CFR 312, 21 CF 812 and divisional policies for the conduct of clinical research.
Management and supervision for all Research Incubator clinical research staff.
Establish professional relationships with Contract Research Organizations, Pharmaceutical Sponsors, Funders and Grantors.
Collaboration with departmental, Research Incubator, and divisional stakeholders for clinical research.
Works with leadership, advisory compliance committee members and research unit leaders to establish a culture of research compliance.
Advises the development of a formalized training program for both new and existing staff within the unit and any affiliates and/or partners.
Plans and manages the protocol review process for all clinical trials which includes the receipt and coordination of protocols for review, committee meetings, and clinical research conferences.
Manages PI and other senior research faculty and personnel, participates as a skilled individual contributor and/or lead researcher as expert in specialized area. Ensures research projects progress according to plan by overseeing the coordination of the daily clinical trial activities.
Performs other related work as needed.
Minimum Qualifications
Education:
Minimum requirements include a college or university degree in related field.
Work Experience:
Certifications:
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Preferred Qualifications
Education:
Master's Degree strongly preferred.
Experience:
Experience with both industry sponsored FDA regulated clinical trial and investigator initiated clinical trial site management.
Regulatory support for FDA
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