• Clinical Trial Manager

    System One (Plainsboro, NJ)
    …deviations, and track trends. + Ensure accuracy and completeness of the electronic Trial Master File (eTMF), supporting inspection readiness and regulatory ... Review Development Safety Update Reports. + Develop the Global Master Informed Consent Form (ICF). + Serve as key...Team issue log in collaboration with the Global Clinical Trial Manager . + Support assessment of … more
    System One (08/08/25)
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  • Clinical Trial Manager - Cambridge

    ICON Clinical Research (Boston, MA)
    …+ Utilizes clinical trial applications including Electronic Data Capture (EDC), Electronic Trial Master File (eTMF), and Clinical Trial Management ... As a CLinical Trial Manager you will be joining...study progress, challenges, and opportunities. **You are:** + Bachelor's/ Master 's Degree in Life Science or equivalent. Experience in… more
    ICON Clinical Research (08/07/25)
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  • Clinical Trial Assistant

    Stanford University (Stanford, CA)
    …of Cell and Gene Therapy clinical trials. This position reports to the Clinical Trial Operations Manager and will support the staff and activities of trials ... Clinical Trial Assistant **School of Medicine, Stanford, California, United...Maintain all forms and documents, including consent forms and master subject logs. File all appropriate correspondence.… more
    Stanford University (08/07/25)
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  • Clinical Trial Specialist

    Caris Life Sciences (Phoenix, AZ)
    …and process fees through accounts payable. + Oversees creation of new study and site Trial Master File (TMF) entries, including site information and required ... yourself, Caris is where your impact begins.** **Position Summary** A Clinical Trial Specialist provides operational and regulatory support for the Caris sponsored… more
    Caris Life Sciences (07/09/25)
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  • Manager Clinical Study Lead (oncology)

    Regeneron Pharmaceuticals (Warren, NJ)
    …study systems including but not limited to Clinical Trial Management System (CTMS), Trial Master File (TMF) etc. + Ensures compliance with the clinical ... role is not eligible to be fully remote._ The ** Manager Clinical Study Lead** (CSL **)** may perform the...masked investigational product, set up and management of unmasked trial master file , review of… more
    Regeneron Pharmaceuticals (08/02/25)
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  • Senior Manager Clinical Study Lead…

    Regeneron Pharmaceuticals (Cambridge, MA)
    …study systems including but not limited to Clinical Trial Management System (CTMS), Trial Master File (TMF) etc. + Ensures compliance with the clinical ... to, assisting with masked investigational product, set up and management of unmasked trial master file , review of unmasked data in the electronic data… more
    Regeneron Pharmaceuticals (08/08/25)
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  • Cyber Identity - Entra ID Specialist Master

    Deloitte (Dayton, OH)
    Job Title: Manager (Microsoft Identity-Entra ID and Active Directory (AD)) Our Deloitte Cyber team understands the unique challenges and opportunities businesses ... role ends on 8/31/2025. Work you'll do As a Manager , you will be at the front lines with...their Active Directory DR plans and perform regular DR trial runs + Monitoring the health of Active Directory… more
    Deloitte (06/07/25)
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  • Sr. Study Manager

    Kelly Services (West Point, PA)
    …and maintaining project schedule and collaborating with Program Lead + Sets up and maintains Trial Master File (eTMF) + Ensures alignment of budget with ... **Senior Study Manager I** **Therapeutic Areas: Oncology & Immunology** **Description...for the following: + Operational point of contact for trial execution and all trial deliverables +… more
    Kelly Services (07/18/25)
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  • Clinical Research Associate, Clinical Monitoring…

    Cordis (Irvine, CA)
    …associated training documentation is available in the site's investigator file and sponsor trial master file + Contribute to the development and review ... Clinical Research Associate (CRA) reports to the Clinical Monitoring Manager . The CRA is responsible for the initiation, maintenance...met per the Clinical Monitoring Plan + Ensuring the Trial Master File is maintained… more
    Cordis (07/09/25)
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  • Senior Clinical Project Manager

    Astrix Technology (Boston, MA)
    …+ Oversee study activities, including reviewing monitoring reports and conducting TMF ( Trial Master File ) checks. + Attend status meetings, ... 10-12 years of professional experience, including at least 3 years as a Clinical Trial Manager (CTM) or Clinical Trial Project Manager . + Previous… more
    Astrix Technology (05/12/25)
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