France Regulatory Submissions Coordinator — Clinical Trials
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Medpace, Inc. is looking for a full-time Regulatory Submissions Coordinator to join our Clinical Operations team in Lyon. This role is crucial for managing the clinical trial process and involves ensuring compliance with regulatory standards.
The ideal candidate will have a Bachelor's degree in a Life Sciences field, with at least 4-5 years of relevant experience. Proficiency in both French and English, as well as strong organizational skills, are essential competencies for this position.
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