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    Senior Director, Us Medical Affairs Solid Tumor Portfolio

    Genmab
    7+ years
    Not Disclosed
    Plainsboro
    10 Nov. 5, 2024
    Job Description
    Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

    Senior Director, USMA Solid Tumor Portfolio - Genmab (Hybrid, Princeton, NJ)

    At Genmab, we are on a mission to build extraordinary futures by developing antibody therapies that transform the lives of patients. We are committed to pioneering treatments that have the potential to change the course of cancer and other serious diseases. Our values are rooted in innovation, science, and a caring, candid, and impact-driven team. We believe that being unique, determined, and authentic is key to fulfilling our purpose.

    The Role: Senior Director, USMA Solid Tumor Portfolio

    As part of the expanding US Medical Affairs (USMA) team, Genmab is seeking an experienced Senior Director to lead the Solid Tumor Portfolio in the U.S. This pivotal role will report directly to the VP/Head of US Medical Affairs. You will be responsible for leading the development and execution of the USMA strategic and tactical plans for our solid tumor portfolio, providing critical market input to the global clinical development and medical affairs programs. You will be instrumental in driving the launch readiness for solid tumor assets and in advancing the overall lifecycle strategy of our portfolio.

    This is a hybrid role, with 60% onsite presence required in Princeton, NJ.

    Key Responsibilities:

    • Lead and build the US Medical Affairs team for the solid tumor portfolio, fostering a high-performance culture and ensuring team success.
    • Develop and execute strategic plans for the solid tumor portfolio, collaborating closely with cross-functional teams.
    • Ensure launch readiness for solid tumor assets, contributing to cross-functional launch activities.
    • Serve as a medical expert for internal and external stakeholders, representing Genmab at major conferences, advisory boards, and training forums.
    • Cultivate strong, collaborative relationships with US thought-leaders and healthcare professionals to gather insights on unmet medical needs.
    • Provide US market input into global clinical development programs and maintain awareness of the competitive landscape.
    • Lead evidence generation strategies, including Phase 3b/4 trials and investigator-sponsored studies (ISTs).
    • Oversee and contribute to the communication of scientific and clinical information to healthcare professionals.
    • Develop partnerships with medical societies, patient advocacy groups, and cooperative groups to gain insights on educational gaps and research needs.
    • Provide leadership, coaching, and performance evaluations for the Medical Affairs team, ensuring continuous growth and development.
    • Collaborate across functions to ensure optimal safety, clinical oversight, and the highest standards in all solid tumor-related work.

    Requirements:

    • Advanced scientific degree (MD, PharmD, PhD, or equivalent), with oncology experience required; gynecologic oncology experience preferred.
    • 10+ years of leadership experience in the pharmaceutical or biotechnology industry.
    • Proven track record of successfully developing and executing medical and scientific strategies to drive product development and commercialization.
    • Strong leadership abilities, with experience in building and managing high-performing teams.
    • Exceptional communication and interpersonal skills to engage with diverse stakeholders.
    • Ability to adapt to changing market dynamics and technological advancements.
    • Regulatory experience is a plus.
    • Willingness to travel up to 30% domestically and internationally.

    Compensation:

    For US-based candidates, the proposed salary range for this position is $255,000 - $425,000, with additional compensation available through bonuses and benefits.

    About You:

    • Passionate about our mission to improve cancer treatment and patient outcomes.
    • Committed to rigor and excellence, with a strong belief in the power of scientific problem-solving.
    • A generous collaborator who thrives in diverse, cross-functional teams.
    • Driven to innovate and embrace challenges in a fast-growing, dynamic environment.
    • Enjoys hard work but also believes in having fun while doing it.

    About Genmab:

    Genmab is an international biotechnology company dedicated to improving the lives of patients with differentiated antibody therapeutics. With over 20 years of experience, we have pioneered next-generation antibody technologies, resulting in a proprietary pipeline that includes bispecific T-cell engagers, immune checkpoint modulators, and antibody-drug conjugates. We are committed to transforming the future of cancer treatment through innovative science and strategic partnerships.

    Commitment to Diversity, Equity, and Inclusion:

    Genmab is deeply committed to fostering diversity, equity, and inclusion in all levels of the organization. We are proud to be an equal opportunity employer and ensure that every applicant is treated fairly, regardless of race, gender, sexual orientation, disability, or any other characteristic.

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