• Clinical Research Coordinator II

    Beth Israel Lahey Health (Burlington, MA)
    …between sponsors and investigators in all aspects of study start up. 3 ) Implements assigned research studies by reviewing study and assessing protocol and ... and communicates study procedures with collaborating departments to ensure compliance with all study requirements; conducts in-services (eg arranges special… more
    Beth Israel Lahey Health (08/01/25)
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  • Assistant Clinical Research Manager - GI Oncology

    Dana-Farber Cancer Institute (Boston, MA)
    …trials using Good Clinical Practice under the auspices of the Principal Investigator . These positions, in collaboration with the program's Clinical research Managers ... group's clinical trial portfolio and all related regulatory and compliance requirements. + Assist the CRM will all aspects...+ Assists the study team to be maintain an " audit ready" research environment **Data Management & Clinical Trial… more
    Dana-Farber Cancer Institute (06/18/25)
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  • Clinical Trials Monitor - Pediatrics

    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 (07/23/25)
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  • Clinical Research Coordinator II

    Dana-Farber Cancer Institute (Milford, MA)
    …clinical trials using Good Clinical Practice under the auspices of the Principal Investigator (s) and the DFCI disease programs. The Regional Campus CRC will be ... to outside entities as required. Maintains site regulatory binders and ensures study compliance with all state, federal, and IRB requirements. May be responsible for… more
    Dana-Farber Cancer Institute (07/30/25)
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