• USMA Regional Medical Scientific Director (RMSD)…

    Merck (Boston, MA)
    …for approved, in-development, and active Company-sponsored trials and/or investigator -sponsored research studies. The Regional Medical Scientific Director serves ... the comprehension of the scientific foundations and goals of investigator -sponsored research + Identifies barriers to patient enrollment and...or MD + Proven competence and a minimum of 3 years of relevant therapeutic area experience beyond that… more
    Merck (05/23/25)
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  • Environmental Monitor/Wetland Protection…

    HNTB (Chelmsford, MA)
    …entirety, providing guidance to less experienced staff. + Prepares and performs environmental compliance monitoring 1 to 3 times per week. Generates field ... for performing field inspections of construction sites to monitor compliance with engineering plans, specifications, and the project's environmental permits.… more
    HNTB (04/22/25)
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  • Clinical Trials Monitor - Breast Oncology

    Dana-Farber Cancer Institute (Brookline, MA)
    …encourage you to apply. + Bachelor's degree in a field relevant to research compliance + 3 + years of progressively responsible clinical trials experience with 1+ ... The Clinical Trials Monitor helps to ensure compliance of the clinical research enterprise with all...including other Harvard Medical School-affiliated hospitals. + Ensure the Sponsor- Investigator and study team adhere to current FDA regulations,… more
    Dana-Farber Cancer Institute (05/08/25)
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  • Associate Director, Clinical Research, Value…

    Takeda Pharmaceuticals (Lexington, MA)
    …Medical Affairs Company Sponsored Studies (MACS) collaborative studies and Investigator Initiated Research (IIR). Specific objectives include: + Partners with ... within assigned TA in accordance with all applicable internal legal and compliance policies as well as external US-specific regulatory guidelines. + Partners with… more
    Takeda Pharmaceuticals (05/03/25)
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  • Research Associate I - Vet Tech

    Tufts Medicine (Boston, MA)
    **Job Overview** This position reports to the Principal Investigator and the Pre-Clinical Surgeon of the Cardiovascular surgical and interventional research ... of experience. **Preferred Qualifications:** 1. Master's degree. 2. Three ( 3 ) years of experience in medical or clinical research...for CV animals housed in the facility. + Ensure compliance with animal use protocols and all other regulations… more
    Tufts Medicine (06/13/25)
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  • Clinical Research Assistant

    Beth Israel Lahey Health (Boston, MA)
    …with physicians, nurses and fellows. Identifies any problems with protocol compliance and notifies principal investigator and/or research nurse. Begins ... Excel, PowerPoint or Access. Previous clinical research project experience preferred.. 3 . Experience with computer systems required, including web based applications… more
    Beth Israel Lahey Health (04/25/25)
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  • Associate Principal Scientist, Toxicokinetics

    Merck (Boston, MA)
    …definitive/Good Laboratory Practice (GLP)], serving as a contributing scientist/principal investigator on toxicity studies, and executing PK/TK strategies to support ... a high standard in accordance with external and internal regulations. + Ensure compliance with GLP, SOPs, and study protocols. + Deliver high quality scientific… more
    Merck (05/17/25)
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  • Oncology Nurse Residency Program - Clinical…

    Dana-Farber Cancer Institute (Boston, MA)
    …2. Analyzes assessment data to develop and support clinically accurate diagnoses. 3 . Plans care by establishing goals with measurable outcomes. 4. Implements the ... in charts as appropriate and communicates observations and findings to protocol investigator , attending physician and other study team members as appropriate 1.… more
    Dana-Farber Cancer Institute (06/12/25)
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  • Calibration Project Engineer

    Lockheed Martin (Chelmsford, MA)
    …within area of assigned responsibility\. Formulates plans for calibration compliance according to company standards, customer contract requirements, and related ... new equipment into the calibration system; acting as lead investigator for risk identification notices, coordinating equipment repairs or...off benefits\. **Schedule for this Position:** 4x10 hour day, 3 days off per week **Lockheed Martin is an… more
    Lockheed Martin (06/06/25)
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  • Head of Solid Tumor Clinical Development

    Astellas Pharma (Cambridge, MA)
    …Solid Tumor Development reports to the head of Oncology Development and has 3 key objectives they would be expected to deliver on: -Development and implementation ... training and quality control, to the highest level of compliance with ICH, GCP and Astellas policies. -Development, mentorship...in pharma or pharma and/ or as a clinical investigator in academia, particularly in the Oncology Solid Tumor… more
    Astellas Pharma (04/22/25)
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