Medical Director

ARTO; À distance; EUR 125 000 - 150 000; Plein temps

Résumé du poste

A leading biotech firm is looking for a Senior Medical Scientist to join their Clinical Development team. This freelance/contract position offers the chance to work in an innovative environment, focusing on medical monitoring, safety oversight, and supporting crucial clinical studies. Candidates should possess an MD and experience in clinical development, preferably in oncology. This full-time role allows for flexible remote working and will initially last until July, with a strong potential for extension.

Qualifications

• MD required.
• Experience in clinical development (pharma/biotech/academic).
• Solid understanding of GCP and clinical trials.

Responsabilités

• Medical monitoring and safety oversight.
• Supporting clinical studies across Pharma's pipeline.
• Reviewing safety data, SAEs, and PV outputs.

Connaissances

Medical monitoring

Clinical studies

Safety data review

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