Regulatory Submissions Associate - Entry Level (France)

Medpace, Inc.; Lyon; On-site; EUR 42,000 - 52,000; Full time

Job summary

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.

Responsibilities

• 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.

Skills

French proficiency

English proficiency

Education

Bachelor's degree in Life Sciences (preferred)

Tools

Microsoft Office

Job description

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