Associate Director, Medical Affairs Strategy

Puesto: Associate Director, Medical Affairs Strategy )
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
Demonstrated strategic thinking skills, with the ability to synthesize complex information, anticipate future needs and translate insights into actionable Medical Affairs strategies
Strong grasp of data interpretation
Local healthcare system/payer landscape familiarity
Ability to travel internationally as required

Desirable

Nominated signatory status or experience acting as a final medical signatory
Registered physician, preferably with the GMC, or pharmacist registered with the General Pharmaceutical Council
Experience contributing to early access to medicines, either in-house or through the Early Access to Medicines Scheme
Extensive oncology experience, with solid tumour experience preferred
Good understanding of the ABPI Code of Practice

Location:

Madrid, Spain — hybrid, 20–30% remote flexibility
The proposed gross annual base salary range for this position, in the primary location, based on a full time schedule is:
EUR
88.536,
The final salary offer will depend on several factors, including your skills,…