Medical Science Liaison France - remote
Proclinical is seeking a Medical Science Liaison to join our client's team in France.
The Medical Science Liaison is an integral member of Medical Affairs Team and is responsible for collaborating with internal and external stakeholders, bringing insights to inform local medical plans and representing the company's Respiratory portfolio as a scientific expert. Must demonstrate a proactive approach and effective communication skills to contribute to the advancement of the product.
Please only apply if you are an experienced MSL with an industry background in respiratory or cystic fibrosis.
Qualifications:
- Advanced degree (PhD, PharmD, MD) strongly preferred; MS in life sciences with extensive MSL experience may be considered.
Experience:
- Minimum 3-5 years of MSL experience in cystic fibrosis and respiratory areas
- Demonstrated success engaging and managing KOLs or high-impact HCPs in a scientific exchange capacity.
- Excellent interpersonal and communication skills with the ability to clearly articulate complex scientific concepts.
- Comfortable working independently and cross-functionally in a fast-paced, evolving environment.
- Willingness to travel extensively (up to 60-70%).
- Identify, engage, and manage relationships with top-tier KOLs and external experts in the Respiratory therapeutic area.
- Serve as the primary medical point of contact for KOLs in France, building strong and credible long-term relationships based on scientific integrity and mutual interest.
- Conduct high-level scientific discussions to communicate relevant clinical and scientific data, including ongoing or completed clinical trials, disease state information, and therapeutic landscape updates.
- Support the Medical Affairs Director with scientific advisory boards, speaker programs, and congress engagement plans
- Collaborate cross-functionally with Clinical Development, Commercial, and Market Access to ensure strategic alignment with Medical Affairs and timely communication of field insights.
- Gather, analyse, and report actionable scientific and competitive intelligence from field interactions to inform internal strategy.
- Ensure compliance with all regulatory and legal requirements, including company SOPs and industry guidelines e.g. ABPI Code of Practice, IPHA/EFPIA Codes of Practice and all relevant regulatory requirements.
- Serve as a resource to investigators and sites involved in company-sponsored clinical trials; assist with site identification, patient enrollment support, and data collection when appropriate
If you are having difficulty in applying or if you have any questions, please contact Opie Inglis at o.inglis@proclinical.com.
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