• Medical Science Liaison - Cutaneous Oncology

    Sun Pharmaceuticals, Inc (Los Angeles, CA)
    …and ensure they are updated on new data + Respond to requests for investigator sponsored research (ISS) proposals and transit them into Sun and present the research ... + Respond to scientific inquires consistent with the MSL compliance standards, + Foster scientific relationships between SUN and...others + Comply with all applicable SUN Health Care Compliance SOPs and US regulations Qualifications: + Doctorate /… more
    Sun Pharmaceuticals, Inc (11/18/25)
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  • Principal Safety Physician (MD)- CAR T Programs

    Gilead Sciences, Inc. (Santa Monica, CA)
    …of our innovative cell therapies, ensuring patient safety, regulatory compliance , and scientific excellence across the product lifecycle. **Key Responsibilities** ... + Serve as the primary author of safety sections in protocols, Investigator 's Brochures, CSRs, DSURs, RMPs, and regulatory documents/responses. + Represent Drug… more
    Gilead Sciences, Inc. (11/15/25)
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  • Research Project Assistant - Family Medicine

    UCLA Health (Los Angeles, CA)
    …and coordinating research activities across one or more studies, ensuring compliance with study protocols, institutional policies, FDA regulations (CFR), and ICH ... tasks to meet project deadlines while collaborating with the Principal Investigator (PI), sponsors, central research teams, and other departments to ensure… more
    UCLA Health (11/15/25)
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  • Research Grant Specialist I -Pathology Group…

    Cedars-Sinai (Los Angeles, CA)
    …education. The Research Grant Specialist I (RGSI) works with the Principal Investigator (PI) and senior-level research administrators to monitor grant accounts and ... a clear understanding of grant budgets and expenditure restrictions. Ensures compliance with all federal, state,, and local agencies including the National… more
    Cedars-Sinai (11/15/25)
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  • Clinical Research Coordinator Associate

    Stanford University (Stanford, CA)
    …implementation of assigned research protocols, ensuring efficiency and regulatory compliance . Key responsibilities will include recruiting and screening subjects, ... other study related documents, and complete study documents/case report forms. + Ensure compliance with research protocols and review and audit case report forms for… more
    Stanford University (11/11/25)
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  • Senior Precision Medicine Associate- FSP

    Parexel (Sacramento, CA)
    …+ Collaborates within cross functional study teams + Presents at investigator meetings and creates training materials (lab manual, sample collection procedures ... (ICF) Specialist and Precision Medicine Operations Lead (PMOL) to ensure compliance with ICF permissions **Operational Support of Biomarker and Exploratory… more
    Parexel (11/08/25)
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  • Senior Scientific Director, Clinical Development…

    AbbVie (Irvine, CA)
    …plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations and ... analysis, interpretation and reporting of scientific content of protocols, Investigator Brochures, Clinical Study reports, regulatory submissions and responses and… more
    AbbVie (11/07/25)
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  • Sr. CRA, Sponsor Aligned, Oncology

    IQVIA (Carlsbad, CA)
    …a pivotal role in monitoring and managing clinical trial sites to ensure compliance with study protocols, regulations, and sponsor requirements. Be at the forefront ... Quality Assurance: Assess site practices for protocol adherence and regulatory compliance , escalating quality issues as needed. Study Progress Management: Oversee… more
    IQVIA (11/06/25)
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  • Senior Ethics and Investigations Partner

    Intuit (Mountain View, CA)
    …will report to the Director, Ethics & Investigations. What you'll do: As an investigator , you will work as part of a dynamic team responsible for investigating ... harassment, retaliation, workplace bullying, and reported financial, expense, and compliance matters. You will manage a caseload of multiple investigations,… more
    Intuit (11/05/25)
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  • Clinical Research Associate (CRA) - A

    ManpowerGroup (Sunnyvale, CA)
    …involves conducting qualification, initiation, monitoring, and close-out visits, ensuring compliance with study protocols, SOPs, and GCP regulations. **Key ... site qualification, initiation, monitoring, and close-out visits. + Verify investigator qualifications, site facilities, and study documentation. + Perform source… more
    ManpowerGroup (10/29/25)
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