Regulatory Submissions Associate - Entry Level (France)

Medpace, Inc.; Lyon; Sur place; EUR 42 000 - 52 000; Plein temps

Résumé du poste

Medpace, Inc. in Lyon is seeking a full-time, office-based Regulatory Submissions Coordinator to join our Clinical Operations team. This role supports the clinical trial management process by preparing and filing regulatory submissions for France and coordinating with study sites to gather required documents.

Entry-level positions with permanent contracts are available for recent graduates. The ideal candidate will have a Life Sciences degree, strong organization, and fluency in French and

Qualifications

• Bachelor's degree in Life Sciences preferred.
• Proficiency in French and English (written and spoken).
• Excellent organization and communication skills with attention to detail.
• Knowledge of Microsoft Office.

Responsabilités

• Prepare, review, and file clinical trial applications for France.
• Communicate with French research sites to collect documents needed before patient enrollment.
• Provide input on regulatory submissions documents and maintain timelines for study start-up.
• Ensure submissions comply with applicable regulations and guidance.
• Advise on changing country regulations and compliance requirements.
• Track submissions and ensure timely filing of documents.

Connaissances

French proficiency

English proficiency

Formation

Bachelor's degree in Life Sciences (preferred)

Outils

Microsoft Office

Description du poste

Medpace, Inc. in Lyon is seeking a full-time, office-based Regulatory Submissions Coordinator to join our Clinical Operations team. This role supports the clinical trial management process by preparing and filing regulatory submissions for France and coordinating with study sites to gather required documents.

Entry-level positions with permanent contracts are available for recent graduates. The ideal candidate will have a Life Sciences degree, strong organization, and fluency in French and