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Medical Director

ARTO

À distance

EUR 125 000 - 150 000

Plein temps

Aujourd’hui
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Résumé du poste

A leading biotech company is seeking a Senior Medical Scientist for a freelance role in Clinical Development. This position offers the flexibility to work remotely while contributing to an innovative pipeline in the biotech field. Candidates must hold an MD and have experience in clinical development, preferably in oncology. The role includes responsibilities such as medical monitoring, safety oversight, and supporting regulatory documentation. Initial contract is until July with a strong potential for extension.

Prestations

Flexible remote working
Potential for contract extension

Qualifications

  • MD required for this freelance contract role in clinical development.
  • Experience in pharma, biotech, or academic settings is needed.
  • Understanding of GCP and clinical trials is essential.

Responsabilités

  • Medical monitoring and safety oversight in clinical studies.
  • Support clinical studies across the pharma pipeline.
  • Review safety data and provide oversight on regulatory documents.

Connaissances

Medical monitoring
Safety oversight
Clinical development
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
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