• Merck & Co. (North Wales, PA)
    Job DescriptionThe Associate Vice President (AVP)/Section Head , Global Clinical Development, Pediatrics will focus on driving strategy, development, and ... Driving License:Hazardous Material(s):Required Skills:Business Development, Business Development, Business Management, Clinical Documentation , Clinical Investigations, … more
    HireLifeScience (07/02/25)
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  • EPM Scientific (San Diego, CA)
    …and external collaborators, including CROs, vendors, and investigator sites. Review clinical documentation for regulatory compliance and inspection preparedness. ... complaints; lead investigations and corrective/preventive actions (CAPAs). Interpret and apply global regulatory requirements and industry standards to clinical more
    Upward (07/12/25)
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  • Intuitive (Sunnyvale, CA)
    …as head technical designer on cross-functional project teams. Translate clinical requirements and user needs to functional and electrical specifications. Work ... potential. Join a team committed to taking big leaps forward for a global community of healthcare professionals and their patients. Together, let's advance the world… more
    Upward (07/11/25)
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  • Clinical Documentation Global

    Sanofi Group (Morristown, NJ)
    **Job Title:** Clinical Documentation Global Head **Location** : Cambridge, MA, Morristown, NJ **About the Job** Are you ready to shape the future of ... be critical in helping our teams accelerate progress. The Clinical Documentation Head is responsible...management strategies and flawless execution of Clinical Documentation deliverables. We are an innovative global more
    Sanofi Group (07/02/25)
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  • Associate Vice President/ Section Head

    Merck (North Wales, PA)
    **Job Description** The Associate Vice President (AVP)/Section Head , Global Clinical Development, Pediatrics will focus on driving strategy, development, and ... Material(s):** **Required Skills:** Business Development, Business Development, Business Management, Clinical Documentation , Clinical Investigations, … more
    Merck (07/02/25)
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  • Global Head of Quality…

    Abbott (Alameda, CA)
    …a significant impact on people's lives. **The Opportunity** Lingo is seeking an impactful Global Head of Quality and Regulatory Affairs to lead our innovative ... Abbott is a global healthcare leader that helps people live more...EU MDR) and oversee internal and external audits. + Documentation and Submissions: Manage the preparation and submission of… more
    Abbott (06/25/25)
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  • Executive Director, Clinical Operations

    Takeda Pharmaceuticals (Boston, MA)
    …Join us as the Executive Director of Clinical Operations reporting to the Head of Global Clinical Development Operations. At Takeda, we are transforming ... objectives. This individual will also be responsible for functional leadership in global clinical operations, including both direct line management (hiring,… more
    Takeda Pharmaceuticals (06/24/25)
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  • Executive Medical Director, Oncology…

    Takeda Pharmaceuticals (Boston, MA)
    …on regional specificities within Therapeutic Area. **ACCOUNTABILITIES:** + Accountable to Oncology Clinical Science Head to provide strategic clinical input ... on assigned clinical studies. + Leads the Global Development Team (US, EU, and others) managing both...trade-offs in regional requirements are well articulated in the global strategy documentation and that stakeholders are… more
    Takeda Pharmaceuticals (04/29/25)
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  • Clinical Research Coordinator (CRC)

    General Dynamics Information Technology (Portsmouth, VA)
    …Trust/Other Required:** NACI (T1) **Job Family:** Research **Skills:** Clinical Study Protocols,Research Activities,Research Protocols **Experience:** 2 + years ... **Job Description:** GDIT's Military Health team is seeking a Clinical Research Coordinator (CRC) to support the Combat Trauma...studies or IACUC animal studies. + Supports the Department Head of CID and is accountable for research related… more
    General Dynamics Information Technology (05/30/25)
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  • Sr AD / Director, Clinical Pharmacology…

    Boehringer Ingelheim (Ridgefield, CT)
    clinical drug development and registration including all necessary processes and documentation , also for complex clinical development projects that represent ... of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate...Pharm methods and strategies. + In alignment with functional head , represents Clinical Pharmacology at internal as… more
    Boehringer Ingelheim (06/14/25)
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  • Lead Associate, Clinical Cell Therapy…

    Bristol Myers Squibb (Devens, MA)
    …apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of ... team. BMS Cell Therapy Manufacturing is seeking a **Lead Associate, Clinical Cell Therapy Manufacturing** that bring enthusiasm, intellectual curiosity, scientific… more
    Bristol Myers Squibb (07/23/25)
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  • Development Physician, Oncology (Medical Director)

    Astellas Pharma (Northbrook, IL)
    …in the Immuno-Oncology group. + Reports to the Medical Lead/disease area strategy head for the given program(s) and is accountable for defining the strategy and ... execution of assigned trials. + Clinical team leader with clear understanding of areas of...and/or reviewing Safety Narratives, Investigator Letters, and other safety documentation for site-reported safety events. + Coordinates with Safety… more
    Astellas Pharma (07/22/25)
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  • Program Manager- Neuroradiology

    University of Washington (Seattle, WA)
    …with the Section Chief of Neuroradiology and their section, the Vice Chair of Global Affairs, and the Vice Chair of Clinical Research.** **POSITION PURPOSE** The ... contact for the Neuroradiology Section, the Vice Chair of Global Affairs, and the Vice Chair of Clinical...central and peripheral nervous system, as well as extra-cranial head and neck. University of Washington is one of… more
    University of Washington (07/19/25)
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  • Associate Director - Supply Chain

    Lilly (Philadelphia, PA)
    …candidate will have a deep understanding of supply chain networks, clinical regulations, global import/export requirements, commercial regulations, timelines, ... + Ensure uninterrupted supply of critical components and consumables to meet global manufacturing needs for commercial and clinical products + Regularly… more
    Lilly (07/22/25)
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  • LifeFlight Critical Care Ground Transport…

    Vanderbilt University Medical Center (Nashville, TN)
    …University Medical Center** : Located in Nashville, Tennessee, and operating at a global crossroads of teaching, discovery, and patient care, VUMC is a community of ... relinquished to the accepting medical facility. Maintains thorough patient care documentation of assessment and intervention throughout the entire transport and will… more
    Vanderbilt University Medical Center (06/10/25)
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  • Sr Director, Medical Affairs

    Gilead Sciences, Inc. (Foster City, CA)
    …Affairs Research (MAR) Leadership Team and will report to the VP, Head of MAR. **Key Responsibilities:** + Ensures operational oversight of Investigator Sponsored ... team, including interactions with CROs + Primary liaison to the Development Clinical Operations group to make sure processes, policies and talent management… more
    Gilead Sciences, Inc. (07/08/25)
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  • Senior Director, Regulatory Affairs - CMC

    Bristol Myers Squibb (Indianapolis, IN)
    …apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of ... and experienced entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals . We are seeking an...CMC (Manufacturing)** . This position will report to the Head of Regulatory Affairs and will oversee and/or manage… more
    Bristol Myers Squibb (07/13/25)
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  • Director, GCP Audits

    Gilead Sciences, Inc. (Parsippany, NJ)
    …and E-system/Digital Audit Heads for Audit related CAPAs. + Stay current with evolving global clinical regulations and guidance. + Support the development of GCP ... + 10+ Years with MS/MA or MBA **PREFERRED QUALIFICATIONs:** + Proficiency in clinical regulatory requirements ( Global ) is a must. + Expert-level experience… more
    Gilead Sciences, Inc. (06/27/25)
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  • US Transplant Medical Program Lead (MPL)

    Sanofi Group (Morristown, NJ)
    …Medical Program Lead (MPL) will, in collaboration with the relevant Medical Head , lead the strategic direction and operational execution of the medical brand ... policies/SOPs/guidance and required external regulations and guidelines. We are an innovative global healthcare company with a focus on immunology that extends to… more
    Sanofi Group (07/16/25)
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  • Manufacturing Associate, Cell Therapy in

    Bristol Myers Squibb (Devens, MA)
    …apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of ... in standard operating procedures and batch records. + Completing documentation required by process transfer protocols, validation protocols, standard operating… more
    Bristol Myers Squibb (07/15/25)
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