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Director of US Medical Affairs Solid Tumors Strategy
2 months ago
We are seeking a highly skilled and experienced Director of US Medical Affairs Solid Tumors Strategy to join our team at Genmab. As a key member of our Medical Affairs team, you will be responsible for providing medical affairs leadership for assigned assets/indications and supporting the overall oncology solid tumor portfolio.
Key Responsibilities- Develop and execute the US Medical Affairs strategy in alignment with the company's goals and meet the needs of the US healthcare market through collaboration with US Commercialization, Global Medical Affairs, Clinical Development, Regulatory, and other cross-functional teams.
- Represent US Medical Affairs as a disease area expert in both internal and external venues, including the US/Global cross-functional teams, clinical development teams, advisory boards, steering committees, professional society meetings, congresses, and local symposia.
- Lead pre/peri/post launch medical activities for assigned assets entering the US market.
- Collaborate with US Field Medical Affairs to identify, guide, and execute disease/indication regional strategies and tactics with appropriate use of resources.
- Work with clinical development, regulatory, commercial, and market access teams to incorporate insights into product strategies and to support product launches and lifecycle management.
- Participate in the evaluation and support of investigator-sponsored trials (IST). Oversee the generation of clinical and real-world evidence in the US that supports the value proposition of our therapies.
- Ensure the effective dissemination of the data generated through publications, presentations, and other communications.
- Provide strategic input and review of congress abstracts, posters, presentation slides, manuscripts, educational materials, advisory board meeting materials, and medical information response documents, etc.
- Build and maintain strong relationships with key US Thought Leaders (TLs), healthcare professionals, and patient advocacy groups to gather insights, drive advocacy, and ensure our therapies meet the needs of patients and healthcare providers in the US.
- Prioritize and monitor US Medical Affairs tactics performance to ensure execution excellence.
- Stay abreast of the latest trends, developments, and competitive landscape in the US healthcare market, particularly within oncology and antibody therapeutics. Use this knowledge to inform and adapt to the US medical strategy as needed.
- Develop a high-performance team. Foster a culture of excellence, collaboration, and continuous learning.
- Advanced degree in a health-related field (MD, PhD, or PharmD preferred). Experience in oncology required.
- At least 8 years of experience in medical affairs, clinical development, or related roles within the biotechnology or pharmaceutical industry, with a strong focus on oncology.
- Experience in the conduct of clinical trials in oncology. Proficiency in clinical data review and interpretation.
- Solid experience in translating medical/clinical information into medical affairs strategies.
- In-depth knowledge of the US healthcare system, including regulatory requirements, payer landscape, and healthcare provider networks.
- Demonstrated customer focus orientation & credibility with customers.
- Excellent communication and interpersonal skills, with the ability to engage and influence a wide range of internal and external stakeholders.
- Strong matrix leadership skills with a track record of building and managing effective teams.
- Ability to navigate and succeed in a dynamic, fast-paced environment with a high degree of collaboration and teamwork.
- Business travel required (~ 35%)
Genmab is an international biotechnology company with a core purpose guiding its unstoppable team to strive towards improving the lives of patients through innovative and differentiated antibody therapeutics. For more than 20 years, its passionate, innovative, and collaborative team has invented next-generation antibody technology platforms and leveraged translational research and data sciences, which has resulted in a proprietary pipeline including bispecific T-cell engagers, next-generation immune checkpoint modulators, effector function enhanced antibodies, and antibody-drug conjugates. To help develop and deliver novel antibody therapies to patients, Genmab has formed 20+ strategic partnerships with biotechnology and pharmaceutical companies. By 2030, Genmab's vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSOTM) antibody medicines.
Established in 1999, Genmab is headquartered in Copenhagen, Denmark, with locations in Utrecht, the Netherlands, Princeton, New Jersey, U.S., and Tokyo, Japan.
We are committed to fostering workplace diversity at all levels of the company and believe it is essential for our continued success. No applicant shall be discriminated against or treated unfairly because of their race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability, or genetic information.
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