Excelya

Senior Medical Writer - Freelancer FR speaking

🇧🇪 Remote, BE Remote Healthcare & Science Contract Senior Posted Apr 30, 2026
LocationRemote, BE
WorkplaceRemote
EmploymentContract
SenioritySenior
CategoryHealthcare & Science
LanguageEnglish
PostedApril 30, 2026
Last verifiedMay 11, 2026

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Key details
1 location, Healthcare & Science, Remote, Senior, Contract
Current openings
19 active jobs
Original language
English
Source and freshness
Collected from public career pages and reviewed through JobGrid.eu source availability checks. Last verified: May 11, 2026.
Apply path
JobGrid.eu sends candidates to the original application page and adds non-personal referral parameters.

Redefine Medical. Empower Innovation. Build with Audacity.

Join Excelya as Our Next Medical Star!

At Excelya, we don’t just work—we Excelyate. Across 24 countries, 900+ passionate professionals are shaping the future of healthcare with one bold ambition: to become Europe's leading mid-size CRO, offering the best employee experience.

Now, we’re calling on curious minds and courageous spirits to step into a career-defining role in Medical Affairs. Ready to make an impact that travels the globe? Let’s talk.

 

About the Job

We are seeking a Freelancer Senior Medical Writer, French speaker for a part-time role, to provide medical and scientific expertise required for the successful completion of Excelya’s projects. The candidate can be based everywhere in EU.

 

Your Mission:

  • Develop, write, and edit a wide range of scientific and medical documents, ensuring accuracy, clarity, and compliance with regulatory and journal requirements.
  • Produce materials such as manuscripts, abstracts, posters, slide decks, and other scientific communications.
  • Prepare and review patient‑facing documents, including:
    -   Informed Consent Forms (FR/ENG)
    -   Non‑opposition letters (FR/ENG)
    -   Lay summaries
  • Write and contribute to clinical and regulatory documents, including:
    -   Clinical study protocols (Phase I–III)
    -   Clinical Study Reports (CSRs)
    -   Common Technical Document sections (CTD 2.4–2.7)
  • Support medical affairs activities such as:
    -   Review of promotional and non‑promotional materials
    -   Medical training for internal and external stakeholders
    -   Medical information services
  • Collaborate with cross‑functional teams, subject matter experts, and clients to ensure scientific accuracy and alignment with project objectives.

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