Medical Director

ARTO; À distance; EUR 60 000 - 90 000; Plein temps

Résumé du poste

A leading biotech firm is seeking a Senior Medical Scientist for their Clinical Development team. This freelance position offers flexible remote working and involves medical monitoring, safety oversight, and supporting clinical studies. The ideal candidate will have an MD, experience in clinical development, and a strong understanding of GCP. This role is critical in contributing to a significant clinical pipeline and supporting studies aimed at market authorization.

Prestations

Flexible remote working

Qualifications

• MD required.
• Experience in clinical development (pharma/biotech/academic).
• Solid understanding of Good Clinical Practice (GCP).
• Comfortable working 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.
• Contributing to clinical and regulatory documentation.

Connaissances

Medical monitoring

Clinical development experience

GCP understanding

Oncology experience

Cross-functional collaboration

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