• Associate Director , GCP

    Takeda Pharmaceuticals (Boston, MA)
    …is true to the best of my knowledge. **Job Description** **ABOUT THE ROLE** The Associate Director , GCP Audit & Compliance provides strategic quality ... adherence to GCP , GCLP, and GVP standards. This role combines audit leadership, supplier oversight, and strategic risk management to enhance end-to-end clinical… more
    Takeda Pharmaceuticals (11/21/25)
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  • Associate Director , Regulatory

    University of Pennsylvania (Philadelphia, PA)
    …through communication of audit results and compliance guidelines. + The Associate Director for Regulatory Affairs will have oversight of regulatory ... of health and wellness programs and resources, and much more. Posted Job Title Associate Director , Regulatory Job Profile Title Associate Director ,… more
    University of Pennsylvania (01/07/26)
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  • Associate Director of Identity…

    NY CREATES (Albany, NY)
    …Category: Administrative Posted On: Fri Dec 5 2025 Job Description: Job Description for Associate Director of Identity and Access Management JOB SUMMARY The ... Associate Director of Identity and Access Management...labs, semiconductor cleanrooms, HPC clusters, cloud workloads (AWS, Azure, GCP ), OT/ICS environments, and federated partner ecosystems. With elite… more
    NY CREATES (12/06/25)
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  • Associate Director , Clinical…

    Takeda Pharmaceuticals (Boston, MA)
    …to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical & Quality Process Compliance is responsible for ensuring ... CPMQ insights on continuous improvement that are enterprise-wide (ie Veeva, QMS, Enterprise Audit , etc.) to Global Quality and R&D Quality. Present to CPMQ at… more
    Takeda Pharmaceuticals (11/14/25)
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  • Associate Director , Data…

    Bristol Myers Squibb (Princeton, NJ)
    …of your application should be directed to Chat with Ripley. R1595700 : Associate Director , Data and Solution Architect Revenue Management Systems **Company:** ... creation and maintenance of technical specifications, process documentation, and SOX/ audit compliance artifacts. + Conduct solution reviews, validate configurations,… more
    Bristol Myers Squibb (01/06/26)
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  • Associate Director of Vulnerability…

    S&P Global (Princeton, NJ)
    …Role:** **Grade Level (for internal use):** 12 S&P Global Corporate **The** **Role:** Associate Director - Vulnerability Management **The Team:** You will be ... 27001, or SOC 2, with demonstrated experience in regulatory compliance and audit management + Exceptional leadership and communication skills, with ability to… more
    S&P Global (12/02/25)
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  • Associate Director , Companion…

    Bristol Myers Squibb (Princeton, NJ)
    …your application should be directed to Chat with Ripley. R1597973 : Associate Director , Companion Diagnostics & Bioanalysis **Company:** Bristol-Myers Squibb ... method, and data lifecycles; steward validated LIMS/ELN records and audit trails. + Serve as the primary liaison for...of FDA QSMR, GLP, CLIA, CAP, ISO13485, IVDR, and ICH- GCP . + Experience with LIMS and electronic data management… more
    Bristol Myers Squibb (01/07/26)
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  • Associate Director , IT

    System One (Princeton, NJ)
    Job Title: Associate Director of IT - Life Sciences/Clinical Location: Princeton, NJ (Mostly remote with some onsite collaboration required - only EST candidates ... compliance with CFR Part 11/GxP regulations including documentation, validation, and audit readiness. + Modernize legacy systems and support digital transformation… more
    System One (12/05/25)
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  • Clinical Trials Operations (CTO) Director

    Morehouse School Of Medicine (Atlanta, GA)
    …trial implementation and performance. The role partners closely with the CRC Associate Director (Physician, Regulatory/Compliance & Fellowship Education) and the ... to ensure operations adhere to institutional policies, ICH - GCP , FDA / OHRP regulations, and payer rules....oversight, and final compliance authority remain with the CRC Associate Director . Minimum Qualifications Master's degree in… more
    Morehouse School Of Medicine (12/18/25)
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  • Associate Director - IWRS Design…

    Lilly (Indianapolis, IN)
    …Help Desk personnel for study set-up and support questions. + Maintain GMP/ GCP compliance by following procedures applicable to clinical trial execution. + Actively ... with Quality to ensure all preparation is complete and reviewed prior to inspection/ audit start. + Successfully operate in, and provide solutions to, complex working… more
    Lilly (12/10/25)
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  • Associate Director - Clinical…

    Lilly (Boston, MA)
    …close-out, ensuring adherence to timelines, budgets, and regulatory guidelines (FDA, EMA, GCP , ICH) using a risk-based approach. + Develop and implement operational ... the planning of quality assurance activities and coordinate remediation of audit findings. + Lead vendor selection, contract/budget negotiation, and management… more
    Lilly (10/31/25)
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  • Director - Cloud Security

    Ford Motor Company (Dearborn, MI)
    …are migrated to Cloud and Software-as-a-Service (SaaS) providers. We are seeking a Director - Cloud Security who will lead a team of security professionals providing ... and policies, ensuring a consistent and effective security posture across Azure, GCP , and all SaaS applications. This includes evaluating, integrating, and managing… more
    Ford Motor Company (11/01/25)
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  • Senior Director , Active Directory

    ADP (Roseland, NJ)
    **ADP is hiring a Senior Director , Active Directory** **Locations: Roseland, NJ or Alpharetta, GA** + _Are you empathetic to client needs and inspired by ... centers** and **public cloud platforms** (Azure, AWS, and possible OCI or GCP ). + Integrate cloud-native identity tools and federated authentication mechanisms with… more
    ADP (11/20/25)
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  • Director for Digital Strategy and Library…

    Stanford University (Stanford, CA)
    Director for Digital Strategy and Library Technology **School of Medicine, Stanford, California, United States** Information Analytics Post Date Oct 30, 2025 ... mission and goals through the management of staff. Reporting to the Associate Dean for Knowledge Management, Stanford Medicine is seeking aDirector for Digital… more
    Stanford University (10/31/25)
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  • Senior Clinical Research Associate

    Parexel (Austin, TX)
    **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials ... in accordance with applicable prevailing laws, Good Clinical Practices ( GCP ), and sponsor standards. The Sr. CRA is accountable...applicable + Serve as a point of contact for audit conduct, and drive Audit Observation corrective… more
    Parexel (12/07/25)
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  • Research Program Coordinator in Precision…

    Stanford University (Stanford, CA)
    …and experienced Research Program Coordinator in Precision Psychiatry.Reporting to the Associate Director of Precision Mental Health Research Programs, the ... local, federal and international regulations on clinical research conduct. + Audit operations to ensure compliance with applicable regulations; provide leadership in… more
    Stanford University (12/16/25)
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  • Regulatory Operations Manager - Pediatrics

    Dana-Farber Cancer Institute (Boston, MA)
    …well as assist with FDA submissions and IND management. Reporting to the CTIP Associate Director for the Pediatric unit, the Regulatory Operations Manager (ROM) ... to monitor and ensure regulatory document collection and maintain compliance and audit -ready state. Assist in audit preparations and represent the department… more
    Dana-Farber Cancer Institute (01/02/26)
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  • Clinical Site Monitor

    University of Utah (Salt Lake City, UT)
    …1. Oversee, coordinate and conduct quality assurance reviews, including monitor and audit visits on cancer related clinical trials to ensure compliance with study ... current knowledge regarding federal and state guidance, including Good Clinical Practice ( GCP ). Disclaimer This job description has been designed to indicate the… more
    University of Utah (01/07/26)
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  • Clinical Research Nurse

    HCA Healthcare (Richmond, VA)
    …human subject research.** **Education & Experience:** + **This position requires an Associate 's Degree in Nursing; Bachelor's Degree is preferred** + **RN license ... to do so** + **Apprises principal investigator, Research Operations Director and Regional Site Manager of all study specific...issues for guidance** + **Assists sponsor and US FDA audit teams** + **Reviews and responds to any monitoring… more
    HCA Healthcare (12/04/25)
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  • Clinical Research Nurse

    HCA Healthcare (Port Charlotte, FL)
    …required or asked to do so + Apprises principal investigator, Research Operations Director and Regional Site Manager of all study specific medical issues for ... guidance + Assists sponsor and US FDA audit teams + Reviews and responds to any monitoring...have:** + Knowledge of federal regulations, good clinical practices ( GCP ) + Knowledge of medical and research terminology +… more
    HCA Healthcare (11/12/25)
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