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Medical Affairs EU Consultant – Cell Therapy (CAR-T) & Lymphoma

Medical Affairs EU Consultant – Cell Therapy (CAR-T) & Lymphoma

LocationParis, France
Business SectorBiotechnology
Contact email
Job ref25172
Published1 day ago
Medical Affairs EU Consultant – Cell Therapy (CAR-T) & Lymphoma
France – Full-time, 1-year contract (Hybrid)

Company Description
A leading biotechnology company with global operations across Europe and the U.S. is seeking an experienced Medical Affairs Consultant to join their expanding EU team. Focused on delivering transformational medicines in oncology and immunology, this biotech is advancing a robust pipeline of small molecules, biologics, and CAR-T therapies for high unmet medical needs. With a decentralized CAR-T manufacturing network and a deep commitment to scientific innovation, the company is reshaping standards in cell therapy and patient care.

Job Description
As Medical Affairs EU Consultant, you will lead regional medical affairs initiatives in France and across the EU, specifically supporting the company’s cell therapy pipeline with a strong focus on CAR-T and lymphoma indications. Your role will involve strategic KOL engagement, medical education, scientific communication, and clinical trial support. You will be instrumental in shaping disease strategies, capturing insights, and aligning medical affairs activities with the organization’s global vision.

Key Responsibilities
  • Build and maintain scientific partnerships with EU-based KOLs, investigators, healthcare providers, and advocacy groups
  • Support recruitment, enrollment, and execution of EU-based clinical trials for CAR-T and other pipeline assets
  • Deliver scientific presentations and medical education to HCPs across France and the EU region
  • Lead disease-area strategies and capture insights from external stakeholders at congresses and scientific meetings
  • Monitor and assess competitive intelligence, market trends, and new data in oncology and cell therapy
  • Review and contribute to medical content: abstracts, posters, training decks, MLR review materials, and response documents
  • Represent EU Medical Affairs at internal meetings, advisory boards, and cross-functional planning sessions
  • Lead the coordination of congress activities and post-congress debriefings
  • Collaborate with internal stakeholders to adapt EU medical materials and training content
  • Ensure medical and scientific communication aligns with regulatory, legal, and ethical standards

Essential Requirements
  • Advanced degree (MD, PharmD, or PhD) in life sciences or a related health field
  • 7–10+ years of experience in Medical Affairs or Clinical Development within biotech/pharma
  • Proven expertise in cell therapy (CAR-T) and lymphoma (Multiple Myeloma experience is a plus)
  • Strong network of KOLs in France and other EU countries
  • Deep knowledge of the EU healthcare system, regulatory frameworks, and payer landscape
  • Strong communicator with the ability to engage a broad range of stakeholders
  • High scientific acumen with experience translating clinical data into medical initiatives
  • Comfortable in a fast-paced, mid-sized biotech environment and cross-functional collaboration
  • Fluent in English (French a strong advantage)
  • Willingness to travel up to 30% (EU-wide)

Additional Details
  • Start Date: ASAP (flexible depending on notice period)
  • Location: France (hybrid; must be based near a major airport)
  • Contract Type: Full-time, 1-year with the possibility of extension
  • Travel: Approx. 30% EU-wide travel required
  • Language: English required; French preferred

Interested
Send your CV to Khanyi Mabena at k.mabena@panda-int.com or reach out directly at +31 44 55 14 407 to learn more.