Entry-Level Study Start-Up Coordinator (May 2027 Grads)

Medpace • Cincinnati, OH, US • published 2026-09-23 11:43:00.911359

Description

Job Summary: Our clinical operations activities are growing rapidly, and we are currently seeking full\-time, office\-based Study Start\-Up Coordinators to join our Regulatory Submissions team. In this position you will work independently and collaboratively to manage timelines, meet goals, and play a key role in the clinical trial management and study start\-up process at Medpace. If you are seeking an **exciting, entry\-level position** where you can build a foundation in the **clinical research industry** and **develop/grow your career** through our robust training program, then this is the opportunity for you. Responsibilities : * Communicate with research sites (doctor's offices, universities, hospitals, etc.) to collect all essential documents required before the site begins to screen patients to participate in the clinical trial; * Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF); * Collect, review, organize, and assemble regulatory start\-up submissions (includes submissions to Institutional Review Boards); and * Maintain timelines for study start\-up through internal team collaboration. **SITE ACTIVATION \& MAINTENANCE (SAM)...

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