Associate Director, Medical Affairs Strategy (Spain)

At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals’ unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees.

Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so.

Does this inspire you and feel like a fit? Then we would love to have you join us!

The Role

Reporting to the Country Medical Director of Spain/Portugal, the Associate Director, Medical Affairs Strategy will be a key scientific and strategic leader responsible for developing and delivering Medical Affairs strategies and tactical plans for assigned oncology assets.

The role will have a particular focus on launch readiness, evidence generation and lifecycle management. Strong strategic thinking skills will be essential to anticipate challenges and opportunities, establish clear medical priorities and shape long-term asset strategy. Working across European and global teams, the Associate Director will translate scientific data, stakeholder insights, patient needs and business priorities into clear medical strategies and impactful activities.

Key Responsibilities

• Develop and deliver Medical Affairs strategic and tactical plans, in collaboration with the Country Medical Director and cross-functional team
• Apply strategic thinking to identify emerging opportunities, anticipate evidence gaps and prioritize activities across launch readiness and lifecycle management
• Acts as subject matter expert in local/regional/global cross-functional teams, clinical development teams, advisory boards and congresses
• Supports pre/peri/post-launch medical activities for assigned asset(s)
• Partners with MSL team for the execution of local Medical Affairs strategies
• Works with Clinical Development, Regulatory, Commercial, and Market Access to shape product strategy and launch/lifecycle plans
• Oversee local data generation strategy
• Review materials for alignment with global and local strategy
• Engages Thought Leaders and patient advocacy groups for insight-gathering

Requirements

• Advanced degree (PharmD, PhD, or MD); oncology experience preferred
• 5+ years in medical affairs, clinical development, or related roles