Sr) Medical Science Liaison, Oncology - Sudostdeutschland

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!

As Medical Science Liaison / Senior Medical Science Liaison for Southeast Germany, you will be Genmab's scientific partner to leading healthcare professionals and researchers within head and neck oncology and other solid tumors.

Working in the field, you will build trusted relationships, facilitate high-quality scientific exchange, and gather insights that help shape our medical and clinical strategies.

You will engage with both approved medicines and investigational assets across Genmab's oncology portfolio. The role combines external scientific engagement with close collaboration across Medical Affairs, Clinical Development, Clinical Operations, and Market Access. You will also support clinical research, medical education, advisory boards, and scientific congress activities.

This is an opportunity to join a passionate, high-impact Medical Affairs team in a dynamic and collaborative environment. Your scientific expertise, communication skills, and understanding of the local healthcare landscape will help advance meaningful collaborations and contribute to better outcomes for patients.

National & international travel required (60% of working time).

• Act as a local expert for Genmab's areas of interest, maintaining up-to-date knowledge of our products, relevant current & evolving clinical landscapes, and the competitive environment.

• Establish and maintain enduring relationships with members of the healthcare/scientific communities who are experts in Genmab's areas of interest.
• Provide appropriate clinical and scientific information on Genmab products in a fair and balanced manner to healthcare professionals (HCPs) in response to unsolicited requests.
• Gather insight into emerging data and evolving clinical practice to inform clinical development and broader strategic initiatives.
• Professionally represent Genmab at selected medical/scientific conferences.
• Offer local expertise to inform engagement of health technology agencies/other payers regarding the value of Genmab products.
• Engage HCPs to advance advisory boards, investigator meetings, & medical education events.

• Collaborate with clinical development and clinical operations teams to support company-sponsored studies, including site identification, feasibility, setup, and recruitment.
• Engage with investigators to advance understanding of company assets and pipeline data.
• Reactively facilitate investigator-sponsored trial proposals, coordinating submission for internal review.

• Align and execute a local territory plan in accordance with EUR/RoW & global MA objectives.
• Inform local publication planning.

• Support training of Genmab colleagues, enhancing their knowledge and understanding of clinical data and our medicines as required.

• Proactively establish effective working relationships with internal cross-functional teams (including medical, development operations, market access) and external partners.

• Advanced Scientific or Medical Degree (Pharm D, PhD, MD) or relevant clinical/professional background required.
• Minimum 2 years of MSL/Medical Affairs experience required, preferably in head & neck oncology; experience of clinical trial conduct is an advantage.
• Proven ability to work independently and as a team player in collaboration with numerous internal cross-functional colleagues.
• Experience of product launch preferred.
• Strong understanding of FSA-Kodex, EFPIA, IFPMA, and other relevant compliance…