• Align and execute local country/regional territory plan in accordance with global MA objectives.
• Translate global MA strategies for Genmab’s clinical development programmes into local country/regional MA strategic plans.
• Act as our local expert on current and evolving clinical landscapes, scientific/healthcare communities, and competitive environment.
• Maintain up-to-date knowledge of products, clinical treatment trends, clinical trials, and scientific activities within Genmab’s haematology/oncology indications of interest.
• Establish and maintain enduring relationships with members of the healthcare/scientific communities who are expert in Genmab’s areas of interest within assigned territory.
• Collaborate with clinical development and clinical operations teams to support company-sponsored studies, including site identification, feasibility, setup, and recruitment.
• Facilitate communications with investigators to advance understanding of company assets and pipeline data.
• Present appropriate clinical and scientific information in a fair and balanced manner to healthcare professionals (HCPs) in response to unsolicited requests.
• Reactively facilitate investigator-sponsored trial proposals, coordinating submission for internal review.
• Engage HCPs as needed to support advisory boards, investigator meetings, medical education activities, etc.
• Provide externally derived insight/feedback to inform development planning and ensure optimal benefit for patients.
• Participate proactively within our Europe & Rest of World medical affairs team, and with both internal cross-functional colleagues and in collaboration with our alliance partners.
• Contribute local/regional advice to inform engagement of health technology agencies/other payers regarding the value of Genmab products.
• Professionally represent Genmab at select medical/scientific conferences.
• Inform local/regional publication planning.
• Support training of Genmab colleagues, enhancing their knowledge and understanding of clinical data and our medicines as required.

• Advanced Scientific or Medical Degree (Pharm D, Ph D, MD) or relevant clinical/professional background required.
• Minimum 1 year of MSL/Medical Affairs experience required, preferably in Haematology/Oncology; experience of clinical trial conduct an advantage
• Proven ability to work independently and as a team player in collaboration with numerous internal cross-functional colleagues and external industry partners.
• Knowledge of relevant pharmaceutical Codes of Practice and other local/regional compliance regulations relevant to interactions with members of the healthcare/scientific community desired.
• Excellent interpersonal communication and presentation skills, strong personal integrity, teamwork abilities, and patient-centric focus are essential.
• Flexible, with positive attitude, strong ability to multi-task, prioritise effectively and communicate at all levels within the company.
• Fluency in French, Dutch & English required; additional languages an advantage
• Demonstrated technical acumen including MS Office skills, ability to adopt and leverage multiple business applications.

• You are passionate about our purpose and genuinely care about our mission to transform the lives of patients through innovative cancer treatment
• You bring rigor and excellence to all that you do. You are a fierce believer in our rooted-in-science approach to problem-solving
• You are a generous collaborator who can work in teams with diverse backgrounds
• You are determined to do and be your best and take pride in enabling the best work of others on the team
• You are not afraid to grapple with the unknown and be innovative
• You have experience working in a fast-growing, dynamic company (or a strong desire to)
• You work hard and are not afraid to have a little fun while you do so