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Study Start - up Coordinator Clinical Research Coordinator Experience
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- Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinators to join our Study Start-up team.
- This position works both independently and collaboratively with a team to meet common goals and plays a key role in the clinical trial management and study start-up process at Medpace.
- Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF);
- Maintain timelines for study start-up through both internal and external collaboration;
- The SAM Training Program embraces evidence based learning & development models to advance professional learning and employee performance.
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