• Oncology Regional Medical Scientific Associate…

    Merck (Boston, MA)
    …and retention efforts to achieve study milestones + Upon request from Global Clinical Trial Operations (GCTO), + Recommends study sites and identifies potential ... License:** Yes **Hazardous Material(s):** n/a **Required Skills:** Advisory Board Development, Clinical Engagement, Clinical Trial Support, Gastrointestinal… more
    Merck (08/23/25)
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  • Research Administrator II - Department of Medicine…

    Tufts Medicine (Boston, MA)
    …competing and non-competing research grant applications, sponsored research agreements and clinical trial proposals, including preparing detailed budgets and ... 2. Identifies all potential costs associated with a proposal. 3. Works with clinical trial teams, creates and negotiates clinical trial budgets with… more
    Tufts Medicine (08/29/25)
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  • Lead Pharmacovigilance QC Specialist

    United Therapeutics (Boston, MA)
    …experience in pharmacovigilance in either case processing or quality assurance of ICSRs ( clinical trial cases & post-marketing reports), OR + Master's Degree in ... in pharmacovigilance in either case processing or quality assurance of ICSRs ( clinical trial cases & post-marketing reports) + 3+ years of experience in vendor… more
    United Therapeutics (08/21/25)
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  • AI-Enabled Early Operational Strategy Lead

    Sanofi Group (Cambridge, MA)
    …organization to identify and rapidly propose and deploy solutions to transform our clinical trial preparation activities globally. + This person will serve as ... of AI solutions that enhance the accuracy, efficiency, and quality of our clinical trial planning. + Collaborate with cross-functional teams to integrate AI… more
    Sanofi Group (08/22/25)
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  • Digital Biomarker Operational Lead - VIE Contract

    Sanofi Group (Cambridge, MA)
    …a pivotal role by identifying, accelerating, and scaling innovations that enhance clinical trial outcomes and experiences for patients, sites, and sponsors. ... management or outsourcing processes would be an advantage. + Understanding of clinical trial processes and terminology would be an advantage. **Education** : +… more
    Sanofi Group (08/13/25)
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  • US Medical Lead, Solid Tumors

    Sanofi Group (Cambridge, MA)
    …documents, ensuring adherence to company standards and government/industry regulations. + ** Clinical Trial Program Management** : Oversee the US medical ... affairs Solid Tumor Oncology clinical trial program, ensuring strategic development of clinical data, including expanded access program + **Product Support**… more
    Sanofi Group (07/29/25)
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  • Global Medical Director, Evidence Generation…

    Sanofi Group (Cambridge, MA)
    clinical studies, RWEs and claims database analyses + In-depth knowledge of clinical trial design, biostatistics, and data analysis. + Proficient in ... as well as study management and publications. + Prior experience in clinical trials, RWE/Epidemiological studies including understanding of trial methodology,… more
    Sanofi Group (07/23/25)
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  • Statistical Project Leader, Deputy Director,…

    Sanofi Group (Waltham, MA)
    …independent data monitoring committees, etc. + May act as the lead statistician at clinical trial level and provide support and leadership to the clinical ... represents the Biostatistics group, and will participate at extended clinical team meetings and may attend external meetings with...and production of statistical reports & appendices at the trial and project level + Manages and follows-up the… more
    Sanofi Group (08/02/25)
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  • Manager, R&D Finance

    Takeda Pharmaceuticals (Cambridge, MA)
    …**POSITION OBJECTIVES:** + Independently leads financial planning, analysis, and reporting for clinical trial costs. + Actively contributes to functional and ... risks, opportunities, and action plans + Track individual department & clinical trial spend + Prepare and distribute timely financial reports with variance… more
    Takeda Pharmaceuticals (06/09/25)
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  • Regulatory Coordinator - Breast Oncology

    Dana-Farber Cancer Institute (Boston, MA)
    …study coordinator, Investigator, DF/HCC QACT, Industry Sponsors, and third party auditors. ** Clinical Trial Management** + Track and manage assigned new protocol ... ensure established benchmarks are met. + Communicate and collaborate with clinical trial key stakeholders through the start-up process, provide regular updates… more
    Dana-Farber Cancer Institute (08/27/25)
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