• Research Administrator II (Post Award)

    Beth Israel Lahey Health (Boston, MA)
    …sponsored research post-award portfolio including oversight and management of financial policy, compliance and reporting issues that arise during the life of the ... to ensure they operate within financial limitations as well as their compliance with legal, sponsor and Center policies and procedures. Position also supports… more
    Beth Israel Lahey Health (06/25/25)
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  • Clinical Research Student Building Bridges

    Beth Israel Lahey Health (Boston, MA)
    …physicians, nurses and fellows. Learns to identify any problems with protocol compliance and notifies principal investigator and/or research nurse. Begins to ... experience in community education and engagement. **Job Description:** **Essential Responsibilities:** 1 . Learns about the process and assists a study team with… more
    Beth Israel Lahey Health (06/06/25)
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  • Clinical Research Coordinator I

    Beth Israel Lahey Health (Boston, MA)
    …by monitoring safety reports, completing start up source documents, maintaining compliance documents, and assisting in protocol feasibility evaluation with principal ... investigator . + Organizes the storage, maintenance, and use of...appropriate documentation for IRB under supervision of the Principal Investigator . Prepares documents for the Committee on Human Studies… more
    Beth Israel Lahey Health (07/30/25)
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  • Research Administrator II (Clinical Research)

    Beth Israel Lahey Health (Boston, MA)
    …trials. Post-award responsibilities involve the administration of research projects in compliance with legal, sponsor and Center policies and regulations. This ... to be part of a remarkable team atmosphere where pre-award, post-award, compliance and research legal work closely together. + Small, single focus institution… more
    Beth Israel Lahey Health (08/01/25)
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  • Clinical Trials Monitor - Pediatrics

    Dana-Farber Cancer Institute (Brookline, MA)
    The Clinical Trials Monitor helps to ensure compliance of the clinical research enterprise with all related regulatory policies and guidelines, including federal, ... and related activities occur as outlined in the monitoring plan and in compliance with all related regulatory standards. Monitoring will be performed through a… more
    Dana-Farber Cancer Institute (07/23/25)
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  • Grant Specialist III, Office Of Proposal, School…

    Boston University (Boston, MA)
    …and ultimately interfacing with the Office of Sponsored Programs (OSP) to compliance review and submission. This position will manage a portfolio of Chobanian ... submission trends to various Deans at BUSM Depending on project, duties will include: 1 . Serve as the administrative lead in the development of all components of a… more
    Boston University (07/15/25)
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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 ... training and continuing education seminars. **Job Description** **Minimum Qualifications:** 1 . Bachelor's degree. (preferred to be in Veterinary Science, Veterinary… more
    Tufts Medicine (07/11/25)
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  • Member Appeals and Grievance Intake Admin…

    Fallon Health (Worcester, MA)
    …(FH) Appeals and Grievance process is an essential function to FH's compliance with CMS regulations, NCQA standards, other applicable regulatory requirements and ... Member Handbook/Evidence of Coverage for all products, and in compliance with applicable NCQA standards and other state or...regulatory standards is required. * Act as the initial investigator and contact person for member grievances and appeals,… more
    Fallon Health (08/01/25)
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  • Director Medical Writing & Clinical Development

    Philips (Cambridge, MA)
    …support medical device performance in alignment with EU regulatory standards (MEDDEV 2.7. 1 Rev. 4, EU Medical Device Regulation). + **Author** and **maintain** ... and Clinical Evaluation Reports, Post-market Clinical Follow-up Plans/Reports, and Investigator Brochures, contributing to Risk Management and Post-Market Surveillance… more
    Philips (07/31/25)
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  • Senior or Principal Pathologist

    WuXi AppTec (Boston, MA)
    …review as SOP and protocol required + Function as a Principal Investigator , responsible for pathology-related activities + Conduct planned, long-term education and ... report. + Provide consultation to Study Directors on studies. + Ensure the compliance of various GLPs, comply with protocol and SOPs during study activities +… more
    WuXi AppTec (07/18/25)
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