• Microbiological/Environmental Monitoring Manager…

    Takeda Pharmaceuticals (Boston, MA)
    …**Job Description** Job Title: Microbiological/Environmental Monitoring Manager and Investigator Location: Lexington, MA **About the role:** Primary duties ... of this position include serving as a lead for various technical aspects of the QC and...contamination investigation regarding impact to lot release for commercial manufacturing . Includes being a subject matter expert for and… more
    Takeda Pharmaceuticals (04/13/24)
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  • Good Clinical Practice (GCP) Senior Quality…

    GE HealthCare (Boston, MA)
    …and Global Compliance support to R&D & GCP activities but also to the GMP manufacturing sites, GDP, PV, and GLP related functions. This role reports directly to the ... Leader Pharmaceutical Diagnostics. The role will oversee, coordinate and lead audits on behalf of PDx QRA with a...R&D functions including to but not limited to CRO's, Investigator sites, Centralised Labs and specialist Non Clinical Labs.… more
    GE HealthCare (05/06/24)
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  • Senior Medical Writer - Oncology

    Merck (Boston, MA)
    …preparing clinical regulatory documents (eg, protocols, clinical study reports, investigator 's brochures, clinical sections of submissions) per company and ... a subset of clinical regulatory documents (eg, clinical study reports, investigator 's brochures, clinical sections of submissions) per regulatory requirements and… more
    Merck (05/25/24)
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  • Medical Science Liaison, Respiratory, Dupilumab…

    Sanofi Group (Boston, MA)
    …of science to improve people's lives. We believe our cutting-edge science and manufacturing , fueled by data and digital technologies, have the potential to transform ... and identifying opportunities for further data collection clinical or investigator -led.** + Monitors disease epidemiology and provides support, including protocol… more
    Sanofi Group (05/19/24)
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  • Regional Medical Scientific Director | IBD…

    Merck (Boston, MA)
    …and goals for approved, in-development, and active Company-sponsored trials and/or investigator -sponsored research studies and serve as a role model for other ... Enhances the comprehension of the scientific foundations and goals of investigator -sponsored research. + Identifies barriers to patient enrollment and retention… more
    Merck (05/18/24)
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  • Director Regulatory Affairs Liaison- General…

    Merck (Boston, MA)
    …and associated documentation. + Provides expertise as the Global Regulatory Lead to Product Development Teams and regulatory single point-of-contact for products ... + Reports to Executive Director or Associate Vice President, Therapeutic Area Lead . + Develops worldwide product regulatory strategy to optimize label and obtain… more
    Merck (05/22/24)
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  • Associate Director- Clinical Trial Management…

    Regeneron Pharmaceuticals (Cambridge, MA)
    …of our new Regeneron Cell Medicines (RCM) group. You will independently lead our clinical study, including planning, maintaining timelines and budgets, vendor ... as well as participating in the development and amendments of protocols, investigator brochures, informed consents, etc. + Performing research site activities, such… more
    Regeneron Pharmaceuticals (05/22/24)
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  • Project Engineer

    Butler America (Chelmsford, MA)
    …of record to enter new equipment into the calibration system, act as lead investigator for risk identification notices, coordinating equipment repairs or ... SAP * Experience working in a defense company with engineering or manufacturing background * Familiarity with functionality of basic electronic components 4x10 First… more
    Butler America (05/21/24)
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