• Clinical Development Lead Prostate (Acp3)

    Bristol Myers Squibb (San Diego, CA)
    …responsible for the design, implementation, monitoring, analysis, and reporting of studies conducted within RayzeBio's portfolio to ensure the program meets the ... and partner with investigators and CROs to design and implement clinical studies + Contribute to writing of protocols, investigator brochures, clinical study more
    Bristol Myers Squibb (11/19/25)
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  • Sr Scientist, Drug Metabolism

    Gilead Sciences, Inc. (Foster City, CA)
    …approaches to optimize study parameters and interpret outcomes. + Prepare study protocols and coordinate execution of nonclinical studies which may involve ... responsibilities include designing and interpreting in vitro and in vivo studies , integrating data into mathematical models, and generating simulations to support… more
    Gilead Sciences, Inc. (11/18/25)
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  • Associate Director, Medical Affairs Statistical…

    Ascendis Pharma (Palo Alto, CA)
    …Associate Director ensures will be working on biostatistics deliverables, including study design, data analysis, data mining, epidemiology-related analyses, use of ... standards, specifications and datasets as needed + Contributes and reviews clinical study protocols, Case Report Forms (CRFs), and internal project plans for… more
    Ascendis Pharma (11/12/25)
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  • Director II, Clinical Innovation, Clinical Design

    AbbVie (Irvine, CA)
    …and creatively apply methodology and analytical skills to bring resolute answers through novel study design. The position may be filled at either the Director I or ... in Irvine, CA. Key Responsibilities + Define objective and develop study design scenarios/options to support novel non-interventional and interventional studies more
    AbbVie (11/19/25)
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  • Executive Director, GCO Franchise Head

    BeOne Medicines (Emeryville, CA)
    …+ Provide guidance to the CST and ensure timely, quality, and efficient study planning and execution of associated clinical programs/ studies + Conduct regular ... lead and manage the Global Clinical Program Lead (GCPL)/ Global Clinical Study Manager (gCSM) group in designated Franchise(s)- therapeutic area (s) or asset(s),… more
    BeOne Medicines (11/07/25)
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  • Executive Medical Director, Product Safety…

    BeOne Medicines (San Mateo, CA)
    …safety Post Approval Commitments (PAC) proposals, facilitates the design of PAC proposed safety study , executes PAC studies + Leads and manages the definition of ... of safety concerns and together with teams engaged in BeiGene sponsored studies , ensures the safety of patients. **Essential Functions of the** **Job:** +… more
    BeOne Medicines (10/24/25)
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  • Heart Institute Clinical Research Assoc I/CPT, Dr.…

    Cedars-Sinai (Los Angeles, CA)
    …to assist in tasks supporting the coordination/implementation of noncomplex research studies . Supports objectives of research studies through noncomplex tasks ... to assist in tasks supporting the coordination/implementation of noncomplex research studies . + Collects, evaluates and/or abstracts clinical research data. May… more
    Cedars-Sinai (12/31/25)
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  • Director, Biostatistics - PK/PD

    BeOne Medicines (Emeryville, CA)
    …provide strategic statistical leadership for pharmacokinetic (PK) and pharmacodynamic (PD) studies across all phases of clinical development. This role partners ... Clinical Biomarker, Regulatory Affairs, and Clinical Development to ensure robust study design, insightful data analysis, and timely support for global regulatory… more
    BeOne Medicines (10/09/25)
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  • Engineer I-II-III-IV

    Ventura County (Ventura, CA)
    …transportation planning, implementing active transportation plans, preparing feasibility studies and reports, preparing grant applications for Federal, State ... material testing firms; the review and or preparation of design studies , plans and specifications, and calculations; executing consultant contracts and managing… more
    Ventura County (12/29/25)
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  • Research Nurse Coordinator I (Hybrid)

    Cedars-Sinai (Beverly Hills, CA)
    …is responsible for all activities associated with clinical study coordination, subject recruitment/enrollment, data management/integrity, regulatory compliance, ... interfaces with participants and family members. Coordinates the clinical logistics of the study , and works in tandem with the Research and/or Clinical Nurse who… more
    Cedars-Sinai (01/04/26)
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