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Clinical contract coordinator

Norwich
Commonwealth of Virginia
Contracts coordinator
Posted: 3 November
Offer description

Title: Clinical Contract Coordinator

Agency: VP FOR RESEARCH

Location: Norfolk, VA

FLSA: Exempt

Hiring Range:

Full Time or Part Time:


Job Description:
The Clinical Contract Coordinator plays a key role in supporting the administrative lifecycle of clinical research agreements within Old Dominion University’s Division of Research and Economic Development (DivRED), Sponsored Programs Administration, which operates through the ODU Research Foundation. Embedded within the Virginia Health Sciences (VHS) Office of Research, this position provides decentralized, on-site support to clinical research teams. Responsibilities include coordinating contract intake and routing, managing documentation, maintaining compliance checkpoints, and supporting the preparation of sponsor funding proposals and study startup materials. The position also contributes to the review of standard agreements, completing amendments for contracts and/or budget documents, as necessary, and tracking contract progress to ensure timely and compliant execution. Well-suited for an early-career professional, the role helps bridge administrative coordination between the Sponsored Programs Administration, DivRED, and the Virginia Health Sciences research infrastructure to support the efficiency and integrity of the clinical research enterprise. Minimum Qualifications:

1. Master’s degree in a general professional or technical field such as finance, business administration or advanced mathematics. Or a bachelor’s degree in the same with work experience equivalent to a master’s degree.
2. Working knowledge of Microsoft Office Suite – Excel and Word required. Experience with research administration is required; experience clinical research administration is preferred.
3. Working knowledge of administrative processes in a professional or academic environment, with a willingness to learn clinical research administration, budgeting principles, and regulatory requirements. Familiarity with clinical trial agreement types (CTA, NDA, DUA) contract lifecycle, and study startup processed preferred but not required.
4. Working organizational and time-management skills to support multiple deadlines, tasks, and maintain accurate documentation.
5. Working problem-solving and critical thinking skills, with the ability to apply logic and judgement when evaluating administrative options or resolving routine issues, while taking a collaborative, team-oriented approach to developing and implementing solutions.
6. Working attention to detail – particularly in reviewing documentation, entering data, and managing compliance.
7. Basic ability to maintain confidential and sensitive information.
8. Certified Research Administration (CRA) certification is preferred but not required.
9. Work requires considerable experience in grant and contract experience.
Additional Considerations:

N/A

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