Global Medical Director, Oncology Strategy & Evidence

Ipsen; Paris; On-site; EUR 180,000 - 240,000; Full time

Job summary

Ipsen is seeking a Global Medical Director for Oncology to serve as the strategic medical leader for Ipsen’s flagship oncology asset, overseeing global medical affairs strategy and lifecycle management for pLGG.

You will develop integrated evidence generation plans, engage with key opinion leaders, and ensure dissemination of scientific information to support the asset’s worldwide footprint, with cross‑functional collaboration across medical, regulatory and marketing.

Qualifications

• Advanced clinical/scientific degree (MD, PhD, or PharmD) or equivalent.
• Extensive oncology experience.
• Extensive global medical affairs experience with late-phase development and lifecycle management.
• Exceptional scientific communication and influencing skills.
• Strong understanding of the regulatory environment for medical affairs.

Responsibilities

• Develop and implement global medical affairs strategy aligned with brand objectives and lifecycle plans.
• Oversee design and execution of global and regional medical studies, including real-world evidence (RWE) and investigator-initiated studies (IIS).
• Establish and maintain relationships with global KOLs, academic institutions, and professional societies to gather insights and foster collaborations.
• Plan and execute scientific advisory boards, symposia, and educational events to support asset’s scientific narrative.
• Collaborate with global and regional medical affairs, marketing, regulatory affairs, and market access to ensure cohesive strategy execution.

Skills

MD/PhD/PharmD

Oncology

Global medical affairs

Late-phase development

Scientific communication

Regulatory knowledge

Influencing skills

Education

MD/PhD/PharmD

Job description

Ipsen is seeking a Global Medical Director for Oncology to serve as the strategic medical leader for Ipsen’s flagship oncology asset, overseeing global medical affairs strategy and lifecycle management for pLGG.

You will develop integrated evidence generation plans, engage with key opinion leaders, and ensure dissemination of scientific information to support the asset’s worldwide footprint, with cross‑functional collaboration across medical, regulatory and marketing.