Regulatory Submissions Coordinator

Medpace overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40 countries. Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinator to join our Clinical Operations team in Lyon. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your, education, previous expertise and can develop and grow your career even further, then this is the opportunity for you. Entry-level positions available for recent graduates. Responsibilities Prepare, review, and file clinical trial applications for France; Communicate with research sites in France (hospitals, etc.) to collect all essential documents required before the site starts to enrol patients to participate in the clinical trial; Provide insightful input on regulatory submissions documents and maintain timelines for study start-up through both internal and external collaboration; Ensure submissions comply with applicable regulations and guidance documents; Advise on changing country regulations and compliance requirements; and Track submissions and ensure timely filing of documents. Qualifications Bachelor's degree (in a Life Sciences field); Good level in English and French in written and verbal communication; Attention to detail; Knowledge of Microsoft® Office; Excellent organization and communication skills, great attention to detail; Hands-on experience preparing, reviewing, and submitting regulatory documentation is beneficial but not necessary. Travel: None Please submit your CV in English.

Location: Lyon, FR

Posted Date: 9/14/2025