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!

REQUIREMENTS

• 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 gynecologic oncology; experience of clinical trial conduct/launch experience as advantages.
• 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 pharmaceutical Codes of Practice or practice and other relevant compliance regulations applicable to interactions with members of the healthcare/scientific community.
• Excellent interpersonal communication and presentation skills, strong personal integrity, teamwork abilities, and patient-centric focus are essential.
• Flexible, with a positive attitude, strong ability to multi-task, prioritise effectively and communicate at all levels within the company.
• Fluency in English required, additional European languages an advantage.
• Demonstrated technical acumen including MS Office skills, ability to adopt and leverage multiple business applications.

Training & Education:

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

THE ROLE

Our Medical Science Liaisons (MSLs) are field-based medical affairs professionals covering various countries or regions across Europe/Rest of World (EUR/RoW). The role requires scientifically trained individuals with strong clinical/scientific backgrounds and excellent communication skills. The MSL / Sr MSL will conduct dynamic medical/scientific exchange with members of the healthcare/scientific community to generate insight and foster collaborations related to both approved and investigational assets within Genmab’s Hematology and Oncology portfolio.
The current role is for an MSL / Sr MSL based in Italy. National & international travel required (60% of working time).
This is an exciting opportunity to be part of the passionate, high-profile, high-impact Medical Affairs (MA) team, and work in a dynamic and collaborative setting.

RESPONSIBILITIES

Scientific Expertise:

• 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.

Medical / Scientific Exchange:

• 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 on 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.

Clinical Trials & Research:

• 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.

Territory Management:

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

Training & Education:

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

Cross-Functional Collaboration:

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