Medical Director

ARTO; À distance; EUR 80 000 - 100 000; Plein temps

Résumé du poste

A leading biotech company is seeking a Senior Medical Scientist for a freelance role in Clinical Development. This position offers flexible remote working options and an initial contract until July, with strong potential for extension. You'll play a key role in medical monitoring, safety oversight, and supporting clinical studies moving towards market authorization. The ideal candidate is an MD with experience in clinical development and a solid understanding of GCP and clinical trials.

Prestations

Flexible remote working

Initial contract with extension potential

Qualifications

• MD required.
• Experience in clinical development in pharma, biotech, or academic settings.
• Solid understanding of GCP and clinical trials.

Responsabilités

• Medical monitoring and safety oversight.
• Supporting clinical studies across Pharma’s pipeline.
• Review safety data and support site interactions.

Connaissances

Medical monitoring

Safety oversight

GCP understanding

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