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Charles City

    Medical Director, Oncology, US Medical Leader - Charles City, United States - TANNER & ASSOC INC

    TANNER & ASSOC INC
    TANNER & ASSOC INC Charles City, United States

    1 week ago

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    Description
    Medical Director, Oncology, US Medical Leader


    The US Medical Organization, Medical Director, Oncology, US Medical Leader is the single point of accountability and matrix leader for US Medical strategies, including US launch and life cycle management.


    The USML is responsible for:
    Leading the development, execution and communication of the US Medical Team (USMT) plan.
    Collaborating with the US Brand Team in the brand/launch planning process to ensure alignment between medical and brand activities
    Data generation in the US (including Ph4, HE, Observational, and NASCR) in partnership with Development Operations, Center for Observational Research and Global Health Economics in support of global development and regional strategies
    Partnering with the Therapeutic Area (TA) field-based, Regional Medical Liaisons (RMLs) and HOPE (Health Outcomes and Payer) RML teams to develop and maintain relationships with external clinical community, including interactions with opinion leaders, payers and medical societies for scientific exchange
    Developing US advocacy plan in partnership with Medical Communications, US Value & Access, and Global Development
    Providing US-focused medical input into global Development strategy, study design and deliverables (e.g., protocol, CSR, manuscript)
    Ensuring consistency of clinical content and scientific messages across publications and materials
    Budgeting and forecast accuracy within area of responsibility
    Coaching, mentoring and developing team members
    Provide interpretation of clinical study data
    Basic Qualifications
    MD or DO degree from an accredited medical school

    AND
    2 years of clinical research experience and/or basic science research in Oncology
    Preferred Qualifications
    Board certified or board eligible
    Clinical research/medical affairs experience in the biopharmaceutical industry (biotech, pharmaceutical or CRO) that includes collaborations with integrated delivery networks, accountable care organizations, and/or payers
    Experience with clinical study management and conduct
    Familiarity with US health care compliance considerations
    Experience with opinion leader interactions
    Experience with integrated delivery networks, accountable care organizations, and payers
    Broad and formal leadership experience
    Knowledge
    Pharmaceutical product development, product lifecycle and commercialization process knowledge with advanced understanding of other functions; including, but not limited to, Clinical Operations, Commercial, Regulatory, and Medical Affairs
    Therapeutic area knowledge
    Network of customer contacts in therapeutic area
    Knowledge of local pharmaceutical industry and legal/health system environment
    Finance/budgeting and resource management experience

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