• Medical Director , Breast Cancer…

    Pfizer (Groton, CT)
    …of Real World Data. + Publication Subcommittee (PSC) Membership: + Collaborate with Clinical Development and Global colleagues on key governance committee to ... brand strategies and tactics, aligning on US regional medical affairs needs. + Lead development of medical strategies and tactics in partnership with Field Based… more
    Pfizer (09/21/24)
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  • Director - Global Biopharma Business…

    Caris Life Sciences (CT)
    …and managing existing and prospective partner relationships. The BBD lead will help drive and develop relationships with existing and prospective partners ... network and connections, as well as expertise, to target partners. The BBD lead will be expected to learn the company's products/solutions, and work with current… more
    Caris Life Sciences (08/05/24)
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  • Senior / Global Medical Advisor - Oncology…

    Boehringer Ingelheim (Ridgefield, CT)
    global matrix teams, regional/local counterparts and external partners. **Requirements for Global Medical Advisor** + MD , PhD or similar (specialist in the ... execution for Evidence Generation. + In case the Sr. Global Medical Advisor acts as Evidence Lead ,...the Asset Evidence sub-team or acting as the Evidence Lead , oversees Clinical Development strategy for the… more
    Boehringer Ingelheim (09/13/24)
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  • Senior Manager, Oncology Early Stage…

    Pfizer (Groton, CT)
    …overall role of the Oncology Early Stage [OES] Clinical Scientist (Senior Manger, non- MD ) is to work collaboratively with the Global Development Lead ... (and members of the development team) to establish, lead , coordinate, and execute the early oncology clinical...addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 17.5%… more
    Pfizer (09/21/24)
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  • Executive Director , Global Medical…

    Merck (Hartford, CT)
    **Job Description** The Executive Director , Global Medical and Scientific Affairs (EDMA) GYN Malignancies is accountable for the development and execution of ... (V&I) plans for their assigned Therapy Areas (TA). They lead a team of TA dedicated global ...**Preferred Experience and Skills:** + At least 5 years global or US medical affairs or clinical more
    Merck (08/27/24)
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  • Asset Quality Lead ( Director )

    Pfizer (Groton, CT)
    …of different regulatory requirements of different sites and countries. + Ability to lead cross-line global initiatives or root cause analysis for quality related ... maintaining 'quality' line-of-sight for assets/protocols within the Pfizer Oncology clinical portfolio. + With this focus, the Asset Quality... portfolio. + With this focus, the Asset Quality Lead (AQL) role brings deep knowledge of Level One… more
    Pfizer (09/21/24)
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  • Director /Senior Associate Director

    Boehringer Ingelheim (Ridgefield, CT)
    …advisory committees, global regulatory authority meetings, Advisory Boards, Board of Managing Directors, congresses. + Lead strategic projects within GPV (eg ... the opportunity for significant professional development. The (Senior Associate) Director is a key member of global ,...as required to ensure safe use in patients. The Director may also lead a team of… more
    Boehringer Ingelheim (07/13/24)
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  • Director , Compound Development Team…

    J&J Family of Companies (Hartford, CT)
    …other key stakeholders. * Represents the interests of the compound/brand along with the global commercial lead at the Oncology SLT. * Builds and maintains team ... Director , Compound Development Team Leader-Oncology - 2406212964W **Description**...**Travel** Yes, 10 % of the Time **Job Function** Clinical Development & Research & Non- MD **Req… more
    J&J Family of Companies (09/18/24)
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  • Director , Regulatory Medical Writing (1…

    J&J Family of Companies (Hartford, CT)
    …practices across R&D. Principal Responsibilities: Leadership: + With a focus on clinical scientific content, lead early strategic submission discussions in ... Director , Regulatory Medical Writing (1 of 4) -...relevant submission documents is required. + Experience leading and managing Regulatory Medical Writing submissions (major global more
    J&J Family of Companies (09/17/24)
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  • HEOR Value Demonstration, Product Director

    Boehringer Ingelheim (Ridgefield, CT)
    …preferred. + In lieu of a doctoral level research degree, a doctoral level professional clinical degree ( MD , DO, PharmD, etc) AND a Master's degree OR other ... overview of our benefits please click here. (https://www.boehringer-ingelheim.com/us/careers/benefits-rewards) **Description** Lead the development, implementation, and communication of HEOR strategies… more
    Boehringer Ingelheim (09/21/24)
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