• Regulatory Operations Manager - Breast Oncology

    Dana-Farber Cancer Institute (Boston, MA)
    …identify priority trials and complete submissions through IRIS. Process protocols through DFCI Institutional Review Board (and other institutions' IRBs). + ... Application (NPA) vetting and prioritization, ensuring that IRIS submission, review and approval timelines / institutional benchmarks...continuing reviews, events, and other submissions for SRC and IRB review and approval. + Manage the… more
    Dana-Farber Cancer Institute (08/27/25)
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  • Clinical Research Coordinator I - Nephrology

    Tufts Medicine (Boston, MA)
    …study sponsor and Institutional Review Board . 5. Assists with Institutional Review Board ( IRB ) requirements for each study including meeting ... institutional educational requirements, submitting documents for review such as amendments, adverse event reporting and annual reviews. 6. Performs basic… more
    Tufts Medicine (08/26/25)
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  • Human Research Quality Manager, School…

    Boston University (Boston, MA)
    …and verify adherence to applicable regulations, laws, and policies and to the IRB approved protocols. This individual conducts on-site and remote reviews of IRB ... significant contact with BMC and BU Medical Campus investigators and the IRB . Excellent presentation, written and verbal communication skills are required. Required… more
    Boston University (07/09/25)
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  • Clinical Research Assistant- Food and Allergy…

    Children's Hospital Boston (Boston, MA)
    …the scheduling of patient visits. + Document preparation and review for the Institutional Review Board ( IRB ) + Processing and storing blood ... and stool samples in the laboratory + Other investigative and administrative duties, as necessary Minimum Qualifications Education: + Bachelor's Degree in STEM or Psychology. Boston Children's Hospital offers competitive compensation and unmatched benefits… more
    Children's Hospital Boston (08/27/25)
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  • Clinical Research Assistant - Urology

    Children's Hospital Boston (Boston, MA)
    …that may arise throughout the study. + Coordinates and prepares the necessary documentation for Institutional Review Board IRB and Committee on Clinical ... reports and analytical summaries for distribution to study research team for review and analysis. Writes articles and summary papers of studies for submission… more
    Children's Hospital Boston (08/26/25)
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  • Associate Director, Breast Oncology Statistical…

    Dana-Farber Cancer Institute (Boston, MA)
    …committees, including but not limited to Scientific Review Committees (SRC) and Institutional Review Board ( IRB ). **Manuscript Preparation:** May ... direct and/or advise junior statisticians in working with investigators to prepare scientific manuscripts. **Grant Preparation:** Expertise in consulting with investigators on all aspects of grant submissions. Work with grants manager on all administrative… more
    Dana-Farber Cancer Institute (08/08/25)
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  • Sr. Clinical Research Coordinator-Emergency…

    Beth Israel Lahey Health (Boston, MA)
    …research nurse, submits protocols, amendments, notices, suspensions and terminations to the IRB for review and approval. (essential) + Interacts with patients ... multiple clinical trials, ensuring compliance with federal, state and institutional guidelines. Financial responsibilities including assisting with the grant… more
    Beth Israel Lahey Health (08/09/25)
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  • Sr. Regulatory Specialist - Clinical Research…

    Beth Israel Lahey Health (Boston, MA)
    IRB . Interact with the FDA on emergency use of a test article without IRB review applications. (essential) + Assist in preparation of FDA, cooperative group ... + Prepare and submit applications, including preparation of consent forms to the IRB on all clinical trials (industry, cooperative groups and PI initiated studies),… more
    Beth Israel Lahey Health (08/21/25)
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  • Regulatory Coordinator - Breast Oncology

    Dana-Farber Cancer Institute (Boston, MA)
    …applications, amendments, continuing reviews, and informed consent documents for SRC and IRB review and approval. + Prepares and submits regulatory documentation ... Create and maintain tracking for all subsequent submissions to the SRC / IRB ; protocol & consent amendments, all required safety reporting, all required deviation,… more
    Dana-Farber Cancer Institute (08/27/25)
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  • Clinical Research Coordinator - GI Oncology

    Dana-Farber Cancer Institute (Boston, MA)
    …the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. + ... and ensures study compliance with all state, federal, and IRB requirements. May be responsible for IRB ...and IRB requirements. May be responsible for IRB protocol submissions (amendments, continuing reviews, and minimal risk… more
    Dana-Farber Cancer Institute (08/27/25)
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