Global Oncology Medical Affairs Director

Ipsen Pharma (SAS); Paris; Hybrid; EUR 150,000 - 200,000; Full time

Job summary

Ipsen Pharma (SAS) is seeking a Director Global Medical Affairs Oncology to lead the global medical strategy for its oncology asset. You will shape evidence generation plans, engage with key opinion leaders, and ensure scientific rigor across the product lifecycle in a global context.

The role requires extensive oncology and global medical affairs experience, with strong scientific communication, regulatory understanding, and cross-functional leadership in a fast-paced biopharma environment.

Qualifications

• Extensive experience in Oncology.
• Extensive experience in global medical affairs within the biopharmaceutical industry.
• Exceptional scientific communication and influencing skills.
• Solid understanding of the regulatory environment governing medical affairs activities.

Responsibilities

• Develop and implement the global medical affairs asset’s strategy, aligning with the overall brand objectives and lifecycle plans.
• Oversee the 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.
• Work closely with global and regional medical affairs teams, marketing, regulatory affairs, and market access to ensure cohesive strategy execution.
• Ensure all medical activities comply with internal policies, Good Clinical Practice (GCP), and applicable regulatory requirements.

Skills

English fluency

Scientific communication

Regulatory understanding

Education

Advanced clinical/scientific degree MD, PhD, or PharmD

Job description

Ipsen Pharma (SAS) is seeking a Director Global Medical Affairs Oncology to lead the global medical strategy for its oncology asset. You will shape evidence generation plans, engage with key opinion leaders, and ensure scientific rigor across the product lifecycle in a global context.

The role requires extensive oncology and global medical affairs experience, with strong scientific communication, regulatory understanding, and cross-functional leadership in a fast-paced biopharma environment.