• Laboratory Supervisor, CMCF

    Dana-Farber Cancer Institute (Boston, MA)
    …Harvard Medical School-affiliated hospitals. + Perform the duties of a Lead Specialist approximately 95% of the time. + Staff Supervision: Overseeing and ... of cell processing protocols, ensuring efficiency, scalability, and adherence to regulatory standards. Is responsible to insure alignment between Sponsor and CMCF… more
    Dana-Farber Cancer Institute (07/08/25)
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  • Research Administrator II (Post Award)

    Beth Israel Lahey Health (Boston, MA)
    …and translate financial data so it is understandable for the non- specialist . Investigate any anomalies and provides timely resolutions. Reallocate budgets and ... sponsored grant activity. Remain abreast of current trends, practices, regulatory and/or policy changes of granting entities, which may...and approvals are met before and after all grant submissions and awards are made, including but not limited… more
    Beth Israel Lahey Health (06/25/25)
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  • Senior Manager, Business Development

    The Brattle Group (Boston, MA)
    …(speaking opportunities, sponsorships, conferences, events, media relations, etc.) + Write submissions for practice and individual rankings and awards + Collaborate ... + Provide strategic oversight and daily support to the Business Development Specialist , ensuring alignment with marketing and growth objectives + Lead performance… more
    The Brattle Group (06/11/25)
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  • BSA Analyst

    Needham Bank (Wellesley, MA)
    …possible cases of fraud and/or Money Laundering. + Ensure that deadlines for regulatory related report submissions are met and that that customer monitoring ... understanding BSA/Compliance and Fraud regulations and requirements. + Assist management in regulatory exams. + Uphold the strict BSA related standards set forth by… more
    Needham Bank (07/31/25)
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  • Senior Clinical Research Director, I&I

    Sanofi Group (Cambridge, MA)
    …structure of the clinical sections of the BLA/CTD, Briefing packages for regulatory meetings, PSP/PIP Supports registrations, label submissions and modifications ... for research projects + Represents his/her project at key regulatory agency meetings as the medical spokesperson for the...Required Qualifications:** + Medical Doctor (MD) preferred: GP or specialist , English fluent (spoken and written) + At least… more
    Sanofi Group (07/06/25)
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  • Appeals and Grievances Program Advisor

    Commonwealth Care Alliance (Boston, MA)
    …and for a full program audit. + Participate in data quality checks for regulatory reporting submissions by verifying data in Guiding Care and identifying missing ... etc + Communicate and work collaboratively with AG Representatives, Resolution Specialist and Management to maintain and improve quality of operations. +… more
    Commonwealth Care Alliance (06/06/25)
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