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Emeryville

    Director, Oncology Program Management - Emeryville, United States - BeiGene

    BeiGene
    BeiGene Emeryville, United States

    3 weeks ago

    Default job background
    Description

    Company Overview:

    BeiGene, Ltd

    (NASDAQ:

    BGNE;


    HKEX:
    is a global, commercial-stage, research-based biotechnology company focused on molecularly targeted and immuno-oncology cancer therapeutics.

    With a team of over 10,000 employees across China, the United States (Cambridge, MA; Ridgefield Park, NJ; Emeryville, CA & San Mateo, CA), Switzerland and Australia, BeiGene is advancing a pipeline consisting of novel oral small molecules and monoclonal antibodies for the treatment of cancer.

    BeiGene is working to create combination solutions aimed at having both a meaningful and lasting impact on cancer patients


    General Description:

    Lead and/or mentor the program management team for oncology clinical development lifecycle management

    Develop and lead global product development strategies

    Establish clear processes for team management and communication

    Drive strategic team decision-making and delivery of team goals and objectives

    Lead process improvement initiatives and optimize team efficiency, quality and performance

    Collaborate with teams to deliver on commitments to the organization and to patients

    Essential Functions of the Job:

    Plan and execute projects in accordance with the global clinical development strategy

    Facilitate alignment with key stakeholders and ensure communication across project teams

    Develop, validate, and maintain project schedules within the enterprise project system

    Plan, track, and manage project milestones, dependencies, and critical path

    Lead and facilitate team planning sessions: develop team charter, define project scope, and ensure global cross-functional alignment

    Implement good project and risk management practices

    Manage process for project budget governance and oversight within oncology

    Liaise with internal and external collaborators to deliver high quality work product, presentations, etc.

    Provide internal project management support to core and sub teams, as necessary

    Coordinate team meeting schedules, prepare agendas and minutes, track action items and progress reports according to project management best practices

    Lead process improvement initiatives, e.g., budget change control, program management dashboards and reports, risk management, etc.

    Assume additional responsibilities and leadership that are commensurate with experience and expertise such as independently providing alliance management for drug development partners, independently leading oversight steering committees

    Minimum Requirements - Education and Experience:

    Bachelor's Degree with 10 + years' experience in clinical and drug development in the
    biotech/pharmaceutical
    industry
    OR

    Master's Degree or above with 7 + years' experience in clinical and drug development in the
    biotech/pharmaceutical
    industry

    5 + years in leadership roles as leader in a multicultural & international (global) portfolio environment is a plus

    Other Qualifications:

    PMP certification a plus

    Supervisory
    Responsibilities:

    Lead and/or mentor program management team

    Computer Skills:

    Efficient in Microsoft Word, Excel, Project, and Outlook

    Travel:

    As Needed


    All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.


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