Medical Science Liaison

il y a 4 jours

Paris, France elemed Temps plein

Role: Medical Science Liaison (6 months)

Location: Remote in France

✉️ Contact: veronica@elemed.eu


The Company

Are you ready for a chance to define and create impactful medical devices? If so, we would love to hear from you. This company is a dynamic leader in the medical devices and pharmaceuticals sector, fostering a collaborative environment where employee happiness and professional growth are paramount.


The Opportunity

Are you passionate about making a real impact in the medical devices field? Do you enjoy collaborative environments where your ideas are valued and your expertise is respected? As a Medical Affairs Manager, you will have the opportunity to mentor and collaborate with partners to ensure the success of medical devices from development to commercialization. This contract will be Interim/Freelance for 6 months.


Your Responsibilities:

Clinical Strategy and Support:

  • Develop and execute medical affairs strategies supporting the development and lifecycle management of products.
  • Provide clinical and scientific input during the development and execution of clinical trials and studies.
  • Collaborate with R&D, regulatory, and marketing teams to ensure clinical data supports product claims and regulatory submissions.

Stakeholder Engagement:

  • Establish and maintain relationships with key opinion leaders (KOLs), healthcare professionals, and clinical investigators.
  • Serve as a clinical and scientific liaison to healthcare providers, answering questions and providing training on the use and clinical benefits of products.

Data Analysis and Dissemination:

  • Analyze clinical study results and real-world evidence to generate scientific insights and publications.
  • Develop and present scientific and clinical data at conferences, symposiums, and meetings.
  • Write and review clinical study reports, white papers, and peer-reviewed journal articles.

Regulation and Compliance:

  • Support regulatory submissions by providing clinical expertise and ensuring all documentation meets regulatory requirements.
  • Ensure compliance with regulations, guidelines, and ethical standards in all medical affairs activities.


Your Qualifications:

  • Experience in medical affairs for medical devices
  • Fluent in French and English
  • Sales-oriented attitude


✉️ If this role interests you, please send your application directly to veronica@elemed.eu.


Please note: Due to the high volume of applications we sometimes receive, our team might not be able to contact each applicant individually regarding the status of their application. If you do not hear from us after 10 days, please consider your application unsuccessful.

Key skills we recruit for: ISO 13485, 21 CFR 820, CE marking, MDR, Medical device regulation, MDD, medical devices, Digital health, 510 (K), PMA, Regulatory affairs, quality assurance, QA/RA, design quality, ISO 14971, combination devices, sterilization, AIMDD, CER, PMCF

Check out more opportunities: Visit Elemed Vacancies Join our Linkedin RA/QA/CL community: LinkedIn Group Want a mentor? Elemed's Mentoring Academy

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