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Medical Affairs Director, Solid Tumors

2 months ago


Plainsboro, New Jersey, United States Genmab Full time
Job Overview

Genmab is seeking a highly skilled and experienced Medical Affairs Director to lead the development and execution of the US Medical Affairs strategy for our Solid Tumors portfolio. As a key member of our team, you will be responsible for providing medical affairs leadership for assigned assets/indications and supporting the overall oncology solid tumor portfolio.

Key Responsibilities
  • Strategic Planning
    • Develop and execute the US Medical Affairs strategy in coordination with Global Medical Affairs and other cross-functional teams.
    • Provide medical affairs leadership for assigned assets/indications and support the overall oncology solid tumor portfolio.
  • Medical Expertise
    • Represent US Medical Affairs as a disease area expert in internal and external venues, including 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.
  • Collaboration and Communication
    • 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 support product launches and lifecycle management.
  • Thought Leadership and Stakeholder Engagement
    • Build and maintain strong relationships with key US Thought Leaders, 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.
    • Provide strategic input and review of congress abstracts, posters, presentation slides, manuscripts, educational materials, advisory board meeting materials, and medical information response documents, etc.
  • Performance Monitoring and Improvement
    • 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.
Requirements
  • Education and Experience
    • 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.
  • Skills and Qualifications
    • 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.