• Research Associate III - Lahiri Lab - Department…

    Cedars-Sinai (Los Angeles, CA)
    …review and remain current on literature as it relates to clinical/research study . This position coordinates all lab and/or clinical activities, including but not ... in mice, oral lavaging the rodents and mice; vaccination and survival studies an measure the permeability constant using quantitative auto radiography. 7.… more
    Cedars-Sinai (01/02/26)
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  • Electrical Engineering Professional Associate

    Jacobs (Los Angeles, CA)
    …telecommunication system, life safety system, photovoltaic (PV) design, campus resiliency study , EV charging infrastructure design, emergency power systems, UPS, and ... compliance with energy efficiency requirements (Title24, COMCheck). Perform power system studies for electrical systems using SKM and ETAP including load flow,… more
    Jacobs (12/19/25)
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  • Director, Global Clinical Operations, Compliance

    BeOne Medicines (San Mateo, CA)
    …direction and expertise to GCO stakeholders for the compliant conduct of study programs; designs, implements and monitors measures to reduce compliance risks and ... BeiGene Quality Management System. + Works collaboratively with global and regional study teams to ensure that proper root cause assessments, corrective and… more
    BeOne Medicines (12/17/25)
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  • Manager, Statistics (Hybrid)

    AbbVie (South San Francisco, CA)
    …. Job Description **This is a hybrid position. Candidates must be local and work out of the San Francisco, CA or North Chicago, IL office preferred. Also ... expertise to support the research and development organization. Specific areas of work may include clinical trials, patient safety, and global medical affairs. The… more
    AbbVie (11/26/25)
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  • Principal Quantitative Clinical Pharmacologist…

    Cytel (Sacramento, CA)
    …advanced statistical methods, you will lead quantitative pharmacology activities for clinical studies . You are excited and enthusiastic, motivate your teams to do ... great work and collaborate easily with your clients. You never...sources, employ statistical methods, produce PK/PD modeling, and align study team on strategy. **As a Principal Pharmacometrician, your… more
    Cytel (10/30/25)
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  • Research Coordinator I

    University of Southern California (Los Angeles, CA)
    …prior to CIC approval, looking specifically at necessity and feasibility of required study tests, at areas pertaining to patient compliance, dose modification and at ... information regarding time or effort to facilitate budget set up.2. Ensures that study is conducted as written so that scientific questions are answered.3. Conducts… more
    University of Southern California (11/19/25)
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  • Research Coordinator II

    University of Southern California (Los Angeles, CA)
    …Pathology Core, etc) to identify potentially eligible participants and obtain study -related data. + Screening potential participants for eligibility and obtaining ... with team members and participating in regular team meetings to track study progress and coordinate schedules Successful Candidates Must Demonstrate: The successful… more
    University of Southern California (12/12/25)
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  • Associate Director, Clinical Pharmacology…

    Taiho Oncology (Pleasanton, CA)
    …Our "People first" approach means we also highly value our employees, who work relentlessly to help execute our mission. Taiho's success is founded on ensuring ... the lives of more and more patients. It's our work , our passion, and our legacy. We invite you...drug development teams. + Lead and manage clinical pharmacology study design, data analysis, data interpretation, and reporting. +… more
    Taiho Oncology (11/13/25)
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  • Senior Epidemiologist, Real-World Evidence (FSP…

    IQVIA (San Francisco, CA)
    …research that informs clinical development, regulatory decisions, and market access. **Responsibilities:** ** Study Lead** : Lead execution of studies to generate ... and accelerate evidence generation to improve patient outcomes. In this role, you'll work closely with one sponsor, gaining deep knowledge of their therapies while… more
    IQVIA (10/29/25)
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  • Regulatory Coordinator

    Actalent (Fountain Valley, CA)
    …, ensuring compliance with applicable guidelines and site SOPs. + Perform catch-up work on backlogged studies to bring documentation and submissions up to ... needed. + Support regulatory compliance for approximately 150 ongoing studies at a small, fast-paced clinical site. + Take...requirements and site-specific policies throughout the lifecycle of each study . Job Type & Location This is a Contract… more
    Actalent (12/30/25)
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