Medical Director

ARTO; À distance; EUR 60 000 - 80 000; Plein temps

Résumé du poste

A biotech company in France is seeking a Senior Medical Scientist for a flexible remote contract role until July, with strong extension potential. The successful candidate will be responsible for medical monitoring and safety oversight, supporting clinical studies, and collaborating with various teams. An MD and experience in clinical development are required, with oncology experience preferred. This position offers a unique opportunity to contribute to a growing clinical pipeline in an innovative environment.

Qualifications

• MD required.
• Experience in clinical development (pharma/biotech/academic).
• Oncology experience preferred but not essential.
• Solid understanding of GCP and clinical trials.
• Exposure to medical monitoring or study-level oversight.
• Comfortable in a fast-moving biotech environment.

Responsabilités

• Medical monitoring and safety oversight.
• Supporting clinical studies across Pharma's pipeline.
• Reviewing safety data, SAEs, and PV outputs.
• Working closely with Clinical Operations, PV, and Regulatory teams.
• Supporting site interactions and investigator queries.
• Contributing to clinical and regulatory documentation.

Connaissances

Medical monitoring

Clinical development

Oncology experience

Understanding of GCP

Cross-functional teamwork

Formation

MD

Description du poste

🔍 Senior Medical Scientist – Clinical Development (Freelance / Contract)

📍 France (Flexible remote) | ⏳ Contract until July – extension likely

I’m currently supporting a client with a search for a Senior Medical Scientist to join their Clinical Development team.

This is a great opportunity to work within an innovative biotech environment, contributing to a growing clinical pipeline and supporting studies moving toward late-stage development and market authorization.

🧬 The Role

• Medical monitoring and safety oversight
• Supporting clinical studies across Pharma’s pipeline
• Reviewing safety data, SAEs, and PV outputs
• Working closely with Clinical Operations, PV, and Regulatory teams
• Supporting site interactions and investigator queries
• Contributing to clinical and regulatory documentation

👤 Profile We’re Looking For

• ✔ MD required
• ✔ Experience in clinical development (pharma / biotech / academic)
• ✔ Oncology experience preferred but not essential
• ✔ Solid understanding of GCP and clinical trials
• ✔ Exposure to medical monitoring or study-level oversight
• ✔ Comfortable working in a cross-functional, fast-moving biotech environment

💼 Contract Details

• ✔ Freelance / Contract role
• ✔ Full-time
• ✔ Initial contract until July (strong extension potential)
• ✔ Flexible remote working
• ✔ Based in France or EU-friendly timezone