• Clinical Development Lead Prostate (Acp3)

    Bristol Myers Squibb (San Diego, CA)
    …milestones and budgets + Translate findings from research and nonclinical studies into clinical development opportunities + Oversee Data Review and Independent ... Data Monitoring Committees + Conduct clinical trials using ethical guidelines relevant to the pharmaceutical...+ US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to… more
    Bristol Myers Squibb (11/19/25)
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  • Sr. Director - Clinical Development

    Lilly (San Diego, CA)
    clinical strategy and clinical plans. + Understand and keep updated with the pre- clinical and clinical data relevant to the molecule. Clinical ... according to guidelines above. + Participate in reporting of clinical trial data in Clinical ...activities by working closely with business unit, brand team, clinical plans manager /project management associates and other… more
    Lilly (12/06/25)
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  • Clinical Research Associate I (Hybrid, Per…

    Cedars-Sinai (Los Angeles, CA)
    …protocol and research objectives. Responsible for completing case report forms, entering clinical research data , and assist with regulatory submissions to the ... Administrator or Research Nurse to coordinate/implement study. + Evaluates and abstracts clinical research data from source documents. + Ensures compliance with… more
    Cedars-Sinai (12/21/25)
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  • Executive Director, Clinical Development…

    Bristol Myers Squibb (San Diego, CA)
    …their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Clinical Development Program Leader sits within Clinical Development, ... dedicated to the effective design and execution of drug development. Clinical Development drives clinical development strategy, design, execution, and… more
    Bristol Myers Squibb (11/21/25)
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  • Assistant Clinical Research Coordinator…

    Stanford University (Stanford, CA)
    …causes. The ACRC will perform administrative support duties related to the collection of clinical data and/or the coordination of clinical studies for lung ... of PACCM principal investigators and both the Research Nurse Manager and the Clinical Research Manager...records and/or perform telephone or in-person interviews to gather data , as needed. + Administer standard study questionnaires and… more
    Stanford University (12/05/25)
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  • Assistant Clinical Research Coordinator

    Stanford University (Stanford, CA)
    …Research Coordinator will perform administrative support duties related to the collection of clinical data and/or the coordination of clinical studies. ... the direction and supervision of the faculty physicians, radiation therapy division manager , and clinical research manager . Stanford University, located… more
    Stanford University (12/18/25)
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  • Lead Clinical Lab Scientist - Sharp…

    Sharp HealthCare (San Diego, CA)
    …Regular **Shift** Night **FTE** 1 **Shift Start Time** **Shift End Time** California Clinical Chemist Scientist License - CA Department of Public Health; California ... Clinical Laboratory Scientist (CLS) Generalist license - CA Department...complete documentation of work orders/issues and scheduled review of data /logs/reports as required by CLIA, CA State, CAP and… more
    Sharp HealthCare (12/14/25)
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  • Sr Associate, Field Clinical Monitoring (US…

    Terumo Neuro (Aliso Viejo, CA)
    …when necessary. + Draft study-specific Monitoring Plans in collaboration with a Project Manager and Clinical Quality Assurance. + Assume Lead Clinical ... and others within the company. 7. Experience using technologies for clinical research (electronic data capture and clinical trial management systems). 8.… more
    Terumo Neuro (12/04/25)
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  • Sr. Clinical Research Associate - FSP

    Parexel (Sacramento, CA)
    …+ Follows quality issue processes by escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance ... SE Region - FL** **ONCOLOGY preferred** **Job Purpose:** The Clinical Research Associate (CRA) has local responsibility for the...as appropriate. + Updates CTMS and other systems with data from study sites as per required timelines. +… more
    Parexel (12/10/25)
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  • Senior Clinical Research Associate - West…

    Parexel (Sacramento, CA)
    …+ Follows quality issue processes by escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance ... The Senior Clinical Research Associate (SrCRA) has local responsibility for...as appropriate. + Updates CTMS and other systems with data from study sites as per required timelines. +… more
    Parexel (12/03/25)
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