Medical Writer - Research & Advisory Board Support, THV, Medical Affairs (Temporary role)

Edwards Lifesciences; Besançon; Sur place; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A leading biomedical company in Besançon is seeking a detail-oriented Medical Writer to join their Medical Affairs team. This role involves developing high-quality scientific content related to Structural Heart Disease, particularly in Transcatheter Heart Valves. Candidates should have a university degree in Life Sciences and proven experience in medical writing. This is a short-term assignment for four months, with potential for extension.

Qualifications

• Proven experience in medical writing, preferably in cardiovascular or structural heart disease.
• Excellent written and verbal communication skills in English; proficiency in German and/or French is a strong advantage.

Responsabilités

• Draft, edit, and finalize scientific documents including study protocols and clinical study reports.
• Prepare materials for advisory boards and summarize outcomes.
• Collaborate with Medical Affairs leads to plan and execute advisory boards.
• Ensure all written materials comply with regulatory and ethical guidelines.

Connaissances

Medical writing

Scientific communication

Attention to detail

Project management

Collaboration

Formation

University degree in Life Sciences

Description du poste

Patients are at the heart of everything we do. As part of our Medical Affairs team, you’ll foster internal and external collaboration to generate and disseminate evidence-based clinical practices to help impact patient lives and advance the quality of care. Your scientific curiosity and passion for patients will help us grow our reach and develop innovative solutions for people fighting cardiovascular disease.

We are seeking a detail-oriented and scientifically grounded Medical Writer to join our Medical Affairs team focused on Structural Heart Disease, with a particular emphasis on Transcatheter Heart Valves (THV). This role will support the development of high-quality scientific content related to research studies and advisory board activities, ensuring scientific accuracy, clarity, and alignment with strategic objectives.

This is a short-term assignment for four months (September - December), with the potential for extension.

How you’ll make an impact:

• Scientific Content Development
• Draft, edit, and finalize scientific documents including study protocols, investigator brochures, clinical study reports, abstracts, and manuscripts.
• Prepare materials for and summarize outcomes from advisory boards, including slide decks, briefing documents, and meeting reports.
• Advisory Board Support
• Collaborate with Medical Affairs leads to plan and execute advisory boards.
• Capture and synthesize expert insights into actionable summaries and strategic recommendations.
• Cross-Functional Collaboration
• Work closely with Marketing, Regulatory, and Commercial teams to ensure consistency and compliance of scientific messaging.
• Liaise with local affiliates and external stakeholders to adapt content for regional needs and regulatory environments.
• Quality and Compliance
• Ensure all written materials meet internal quality standards and comply with applicable regulatory and ethical guidelines.
• Maintain version control and documentation for all deliverables.
  

This is a short-term assignment for four months (September - December), with the potential for extension.

What you'll need (Required):

• University degree in Life Sciences (e.g. Biomedical Sciences, Biology, Pharmacy, etc.)
• Proven experience in medical writing, preferably in cardiovascular or structural heart disease.
• Excellent written and verbal communication skills in English; proficiency in German and/or French is a strong advantage.
  
  

What else we look for (Preferred):

• Familiarity with clinical research processes and medical affairs activities.
• Strong organizational skills and attention to detail.
• Ability to manage multiple projects and deadlines in a dynamic environment.
• Experience supporting advisory boards or scientific events in Europe.
• Knowledge of THV technologies and the clinical landscape of structural heart interventions.
• Understanding of local regulatory and compliance requirements in Europe.
  
  

Aortic stenosis impacts millions of people globally, yet it often remains under-diagnosed and under-treated. Edwards’ groundbreaking work in transcatheter aortic heart valve replacement (TAVR) pioneered an innovative, life-changing solution for patients by offering heart valve replacement without the need for open heart surgery. Our Transcatheter Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence. It’s our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.