• Principal Scientist

    Merck (Upper Gwynedd, PA)
    **Job Description** We are seeking a Director ( Principal Scientist ), Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that can ... our pipeline and drive our strategic priorities. The Director , Principal Scientist | Regulatory Affairs Liaison is responsible for development and… more
    Merck (03/19/25)
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  • Associate Principal Scientist

    Merck (Upper Gwynedd, PA)
    **Job Description** **Title: Associate Principal Scientist /Associate Director , Outcomes Research** **Role Summary** + Under the guidance of a senior leader, ... an Associate Principal Scientist /Associate Director , has primary...reimbursement and market access, and provide input into clinical, regulatory , payer/access, marketing and evidence generation strategy and programs… more
    Merck (03/20/25)
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  • Principal Scientist

    Merck (Upper Gwynedd, PA)
    **Job Description** In this Principal Scientist / Director position within Translational Oncology, this team member will provide leadership for aligned and ... Teams (ADTs) and our diagnostic partners. Position reports to Executive Director , CDx. **Primary Responsibilities** : + Direct CDx/IVD development projects,… more
    Merck (03/19/25)
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  • Principal Scientist - Device…

    Merck (West Point, PA)
    …ensure products and processes are developed in accordance with applicable regulatory , quality, company, and customer requirements. This position will lead ... and influence clinical and commercial combination product development and launches. ** Principal Responsibilities** + Lead and set direction for the device… more
    Merck (02/14/25)
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  • Senior Principal Scientist

    Bristol Myers Squibb (Princeton, NJ)
    …oncology. + Manage relationships with key internal stakeholders including regulatory , clinical and commercial and scientific communications and external ... human genetics, immunology). + Minimum of 6 years post-PhD experience for Sr. Principal Level (and minimum of 8 years Post-PhD experience for AD Level), with… more
    Bristol Myers Squibb (03/14/25)
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  • Associate Principal Scientist

    Merck (North Wales, PA)
    …to reimbursement and market access, and provide input into clinical, regulatory , payer/access, marketing and evidence generation strategies and programs. + In ... collaboration with internal teams and external partners, design studies, author study protocols, develop measurement questionnaires, case report forms, data analysis plans, final study reports, scientific presentations, and publications. + Responsible for… more
    Merck (03/20/25)
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  • Senior Principal Scientist

    Merck (North Wales, PA)
    …talented and dedicated colleagues while developing and expanding your career. The Senior Director (Sr. Principal Scientist ) has primary responsibility for ... of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, The Senior Director more
    Merck (03/09/25)
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  • Principal Scientist , Analytical R&D

    Merck (West Point, PA)
    …Cell Based Sciences Department in West Point, PA is seeking a Principal Scientist with technical expertise in developing, characterizing, and implementing ... commercialization. In this role, an individual will work, closely, with the group Director leading a team of scientists to develop technical, scientific, and … more
    Merck (03/04/25)
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  • Principal Medical Science Liaison, US…

    Gilead Sciences, Inc. (Philadelphia, PA)
    …aspirations. Join Gilead and help create possible, together. **Job Description** This field-based Principal Medical Scientist will be part of a team of Medical ... Scientists reporting to a Field Director . The MS will disseminate clinical information about Gilead's...be determined by education and years of experience. A Principal Medical Scientist requires 8+ years of… more
    Gilead Sciences, Inc. (02/15/25)
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  • Director , Early Clinical Develpment…

    Bristol Myers Squibb (Princeton, NJ)
    …and acting on clinical trial data to support development + Serving as principal functional author for Regulatory submission, study reports, and publications + ... lifecycle + Manages site interactions in partnership with the Clinical Scientist for medical questions and education (including safety management guidelines) +… more
    Bristol Myers Squibb (03/13/25)
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