Clinical Research Coordinator
$145,000–$155,000 year
On-siteBethesda, Maryland, United States
Job Summary
Coordinate operational activities for clinical studies, including feasibility assessments, startup support, and multi-center site coordination. Monitor study progress, enrollment metrics, and project schedules while developing and maintaining project management plans. Provide comprehensive oversight of assigned clinical research portfolios, track performance metrics, and facilitate project meetings and documentation. Lead development of work plans, coordinate initiation and closeout activities, and develop risk mitigation plans to ensure alignment with organizational objectives. Serve as a liaison between research programs, regulatory offices, and collaborating institutions to facilitate communication and support audit preparations. Prepare monthly activity, portfolio status, and financial status reports, and assist leadership with prioritization and strategic planning initiatives.
Required Qualifications
- Master's degree
- Health and Medical Administrative Services
- Nursing
Desired Qualifications
- SOCRA Certification
- FAC-P/M Certification
- FAC-COR Certification
- PMP Certification
- Association of Clinical Research Professionals (ACRP)
- Experience with clinical trial management systems and research databases
- Experience with technology transfer agreements, clinical trial agreements, cooperative research and development agreements, or related research partnerships
- Experience supporting NIH, NCI, academic medical centers, or federally funded research programs
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