Senior Medical Writer - Freelancer FR speaking

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 FreelancerSenior 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.

Requirements

What You Bring to the Table:

We are looking for candidates who embody our values of Audacity, Care, and Energy and also:

• Degree in Life Sciences.
• Previous working experience in the pharmaceutical/health industry.
• Experience in writing: ICF (FR/ENG), non-opposition letters (FR/ENG), lay summaries, posters/manuscripts, protocols (Phase I-III), CSR. CTDs (2.4-2.7).
• Experience in medical device-related documents would be considered a plus (CEP/CER/PMCF/PSP).
• Able to work autonomously.
• Experience in clinical documents for interventional and non-interventional studies.
• Critically evaluate scientific data.
• Project management skills.
• Able to review TFLs and participate in data review meetings.
• Fluent in English and French language.

Benefits

Why Choose Excelya?

At Excelya, we lead with Audacity, act with Care, and move with Energy. We nurture your potential through high-impact projects, give your talents the space to shine, and push boundaries to elevate every patient’s journey. Here, you're not just doing a job—you’re becoming a key part of something bigger.

So, if you're ready to excel with purpose, let’s write the next chapter together.