Regulatory Submissions Coordinator — Entry Level (France)

Medpace

Lyon

Sur place

EUR 45 000 - 60 000

Plein temps

14 jours+
Générateur de candidature

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Résumé du poste

Medpace is seeking a Regulatory Submissions Coordinator for our Clinical Operations team in Lyon, France. This full-time, office-based role supports regulatory submissions and trial start-up activities for France, collaborating with sites and internal teams.

Fluency in French and English is required, with a life sciences background ideal for this position. Recent graduates may apply for entry-level positions with a permanent contract.

Qualifications

  • Bachelor's degree (preferably in a Life Sciences field).
  • Excellent organization and communication skills, great attention to detail.

Responsabilités

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

Connaissances

Organization
Communication
Attention to detail

Formation

Bachelor's degree in Life Sciences

Outils

Microsoft Office

Description du poste

Medpace is seeking a Regulatory Submissions Coordinator for our Clinical Operations team in Lyon, France. This full-time, office-based role supports regulatory submissions and trial start-up activities for France, collaborating with sites and internal teams.

Fluency in French and English is required, with a life sciences background ideal for this position. Recent graduates may apply for entry-level positions with a permanent contract.

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