France Regulatory Submissions Coordinator — Clinical Trials

Medpace, Inc.; Lyon; Sur place; EUR 40 000 - 55 000; Plein temps

Résumé du poste

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.

Qualifications

• Minimum of 4-5 years of experience as a Regulatory Submissions Coordinator.
• Hands-on experience preparing and submitting regulatory documentation.
• Full professional proficiency in French and English.

Responsabilités

• Prepare and file clinical trial applications for France.
• Ensure submissions comply with applicable regulations.
• Advise team members on changing regulations.

Connaissances

Regulatory documentation preparation

Bilingual communication (French & English)

Attention to detail

Organization and communication

Formation

Bachelor's degree in a Life Sciences field

Outils

Microsoft Office

Description du poste

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.