• Global Medical Evidence - Integrated Evidence…

    Takeda Pharmaceuticals (Boston, MA)
    …within the CoE of Global Medical. + Provides innovative thinking and scientific expertise into peri- and post-approval research programs and real-world evidence ... of a strategy for all study types within Global Medical, ie Medical Affairs Sponsored Studies (MACs). Also, develops Areas of Interest (AOI) for Collaborative… more
    Takeda Pharmaceuticals (08/12/25)
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  • Precision Medicine Director - Obesity…

    Amgen (South San Francisco, CA)
    …As a key translational thought leader, you will integrate cutting-edge scientific insights with strategic decision-making, steering the development of innovative ... Discovery Research, Clinical Pharmacology, Toxicology, Early Development, and Regulatory Affairs teams to ensure seamless progression from IND-enabling activities… more
    Amgen (08/08/25)
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  • Associate Director, Statistics

    AbbVie (North Chicago, IL)
    …of work may include clinical trials, patient safety, and global medical affairs . The Associate Diector works in partnership with experts in multiple disciplines ... leadership for design, analysis and reporting for clinical or other scientific research programs. Independently develop protocols and statistical analysis plans (or… more
    AbbVie (08/01/25)
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  • Head of R&D and External Innovation Communications…

    Takeda Pharmaceuticals (Cambridge, MA)
    …The Global R&D Communications Team is responsible for advancing Takeda's scientific thought leadership demonstrating the impact of the organization's work, ... to increase the awareness and understanding of our pipeline, partnerships, scientific platforms and business performance. + Shape content strategy and development… more
    Takeda Pharmaceuticals (07/24/25)
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  • Analytical Scientist II

    Herbalife (Torrance, CA)
    …skincare. The position collaborates cross-functionally with R&D, QA, and Regulatory Affairs , while mentoring junior scientists and driving scientific ... + Contribute to audit readiness and documentation accuracy. + Draft scientific publications, validation protocols, and technical reports. + Represent the company… more
    Herbalife (06/21/25)
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  • Senior Medical Writer

    Abbott (Plymouth, MN)
    …The Medical Writer will be responsible for producing abstracts, manuscripts, scientific publications, and clinical study reports. This position will work ... position will work closely with cross-functional stakeholders in marketing, medical affairs , clinical affairs , biometrics, project management, data management,… more
    Abbott (09/12/25)
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  • Head of Safety and Pharmacovigilance - Cell…

    Gilead Sciences, Inc. (Foster City, CA)
    …action moves us one step closer to our goal. We've made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the ... and executive-level forums. This leader ensures global regulatory alignment, scientific excellence, and operational rigor in all safety-related activities, while… more
    Gilead Sciences, Inc. (09/09/25)
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  • Vice President, Global Program Lead Neuroscience

    Bristol Myers Squibb (Princeton, NJ)
    …maximize program impact + Actively supports Investor Relations and Public Affairs in managing external BMS communications **Integrates commercialization inputs and ... the relationship to clinical trial design + In partnership with Medical Affairs , supports development of KOL plans and engagements, and leverages KOL input… more
    Bristol Myers Squibb (08/29/25)
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  • Clinical Development Physician, Oncology (Medical…

    Astellas Pharma (Northbrook, IL)
    …medical affairs and commercial strategies. + Creates and maintains scientific /clinical networks and seeks external opinion leader as appropriate. Serve as the ... medical safety, Toxicology (early phase programs) regulatory, biostatistics, medical affairs , Health Economics, commercial perspectives into clinical development strategies… more
    Astellas Pharma (08/29/25)
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  • Director / Senior Director Medical Writer

    System One (Cleveland, OH)
    …you will be responsible for document creation across clinical development and medical affairs . It is expected this will include the successful preparation of high ... collaboration with cross-functional study teams. Your collaboration with the medical affairs team on publication strategy and execution, in alignment with applicable… more
    System One (08/03/25)
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