• Senior Trial Master

    Rhythm Pharmaceuticals (Boston, MA)
    …tenacity to overcome barriers, together. Opportunity Overview Rhythm Pharmaceuticals, Inc. is seeking a Senior Trial Master File (TMF) Specialist to join ... an integral member of the Clinical operations team, reporting to the Senior Director of Clinical Process and Quality-Control Management, (CPQM). This position will… more
    Rhythm Pharmaceuticals (01/09/25)
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  • Senior Manager, Clinical Trial Tools…

    Takeda Pharmaceuticals (Boston, MA)
    …and oversight models. + Confirm archival and inspection readiness of all Clinical Technology Trial Master File (TMF) documents. + Participate in preparing ... to inspire you and empower you to shine? Join us as a Senior Manager, Clinical Trial Tools & Technologies based remotely reporting to the Clinical Trial more
    Takeda Pharmaceuticals (12/06/24)
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  • Senior Manager, Business System Lead

    Takeda Pharmaceuticals (Boston, MA)
    …experience in clinical trial management/operations preferred. + Expert level expertise with trial master file technology. + Expert level expertise with ... company to inspire you and empower you to shine? Join us as a Senior Manager, Business System Lead based remotely reporting to the Director, Structured Content… more
    Takeda Pharmaceuticals (12/22/24)
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  • Research Project Manager - Dana-Farber Network

    Dana-Farber Cancer Institute (Brighton, MA)
    …oversight and management of assigned projects. + Responsible for development and maintenance of Trial Master File (TMF). + Initiates, plans, facilitates and ... sponsor activities for assigned clinical trials Sponsor activities include coordinating trial startup and site startup activities, safety event tracking and… more
    Dana-Farber Cancer Institute (11/02/24)
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  • Clinical Research Director

    Sanofi Group (Cambridge, MA)
    …raised by EC/IRBs, sites + Develop the clinical study report + Support CRD trial master file documents readiness and availability, and mandatory trainings ... Ensure continuous medical review of aggregated data during clinical trial conduct (DRSR, safety, stat outputs of blinded data,...knowledge of the study, compound, protocol + TA Experts, senior CRDS, global clinical lead, GPHs and medical affairs… more
    Sanofi Group (12/11/24)
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