Entry-Level Regulatory Submissions Coordinator

Prepare, review, and file clinical trial applications for France while communicating with research sites to collect essential enrollment documents. Provide input on regulatory submissions, maintain timelines for study start-up through internal and external collaboration, and ensure submissions comply with applicable regulations and changing country requirements. Track submissions to guarantee timely filing of documents. This entry-level role supports the Clinical Operations team at Medpace, a full-service CRO accelerating global development of safe and effective medical therapeutics across oncology, cardiology, and other therapeutic areas.