• Senior Study Monitor

    Gilead Sciences, Inc. (Foster City, CA)
    …a difference in the world - Being Here Matters. We are seeking an experienced study monitor to complement our Nonclinical Safety (ie, Toxicology) team. ... + Independently monitors and coordinates all aspects of outsourced nonclinical safety studies (eg, calculating test material... study archival). + Independently serves as lead study monitor for IND programs, including responsibilities… more
    Gilead Sciences, Inc. (08/17/24)
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  • Non-Clinical Study Manager

    Astellas Pharma (South San Francisco, CA)
    Study Manager is to select Contract Research Organizations (CROs) and monitor non-GLP and GLP-outsourced nonclinical studies for Astellas Gene Therapies ... harnessing AGT core competencies in AAV gene therapy, the Nonclinical Studies Manager will be responsible for...collaborators. + Review, edit, and finalize non-GLP and GLP nonclinical study protocols, amendments, and reports, ensuring… more
    Astellas Pharma (07/02/24)
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  • Senior Toxicology Report Development Lead

    ICF (Reston, VA)
    …Experience as study director and/or study monitor for nonclinical or hazard identification studies . + Familiarity with data tracking system outputs ... growth and expanding client base, we are seeking a ** Senior Toxicologist** to work in our Health Science Portfolio....NIEHS) in conducting and reporting the results of hazard studies and supporting risk assessments of environmental pollutants and… more
    ICF (09/11/24)
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  • Executive Director, Research QA

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …addressed and managed appropriately. Ability to exercise influence at the senior leadership and/ or executive level wherever GLP/non-GLP/ research programs impacting ... matters and lead any remediation efforts. **Responsibilities** + Leads nonclinical QA function to implement a quality system in...the QA review and approval of GLP and GCLP study protocols, clinical study reports, ICFs, external… more
    Daiichi Sankyo Inc. (08/02/24)
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