University of Chicago
Clinical Research Coordinator 2, MOSAAIC Study for Asian Americans
Chicago, IL, USA · Mid · Contract
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About the role
- The study collects data across a broad range of health domains, including heart health, diabetes, lung health, and mental health, as well as social determinants of health such as environmental exposures and access to care.
- This at-will position is wholly or partially funded by contractual grant funding which is renewed under provisions set by the grantor of the contract.
- Employment will be contingent upon the continued receipt of these grant funds and satisfactory job performance.
Responsibilities
- Support operational execution of multi-institutional and some international studies, many of which are federally funded or funded by pharmaceutical sponsors.
- Manage IRB submissions, amendments, and continuing reviews
- develop and refine data collection instruments
- and deliver continuous milestone reporting - including progress, successes, and emerging challenges - to study leadership.
- Drive participant engagement through active coordination of subject screening, recruitment, informed consent, data and specimen collection, and longitudinal follow-up and retention strategies.
- Manage IRB submissions, amendments, and continuing reviews; develop and refine data collection instruments; enforce implementation accuracy and study staff protocol compliance; and deliver continuous milestone reporting - including progress, successes, and emerging challenges - to study leadership.
- Facilitates and participates in the daily activities of moderately complex clinical studies and performs various activities including patient data retrieval, documenting clinical research records, and participation in program audits.
- Performs other related work as needed.
Requirements
- include a college or university degree in related field.
- Experience coordinating observational and/or interventional clinical research studies, including familiarity with both clinic-based and community-based research settings.
- Demonstrated experience with IRB submissions, amendments, continuing reviews, and related regulatory documentation.
- Experience conducting or supporting study-related procedures such as participant interviews, phlebotomy, and structured follow-up assessments.
- Uses knowledge of clinical studies to coordinate the collection of analyzable clinical research data and/or samples with a limited to moderate degree of independence.
Nice to have
- Prior work on multi-site, federally funded, or industry/pharmaceutically sponsored research studies
- experience with international studies a plus.
Compensation
- $60,000.00 - $75,000.00 The included pay rate or range represents the University's good faith estimate of the possible compensation offer for this role at the time of posting.
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Benefits
- Yes The University of Chicago offers a wide range of benefits programs and resources for eligible employees, including health, retirement, and paid time off.
- Information about the benefit offerings can be found in the Benefits Guidebook.
Equal opportunity
- Job seekers in need of a reasonable accommodation to complete the application process should call 773-702-5800 or submit a request via Applicant Inquiry Form.
- Job seekers in need of a reasonable accommodation to complete the
Visa & Work Authorization
- quisition, entry, QC, and query response, ensuring timely and accurate data flow in compliance with study protocols and sponsor or regulatory requirements
This listing is sourced directly from University of Chicago's careers page and normalized into a canonical job model.