• Regulatory Affairs Process Specialist

    Kelly Services (Sunnyvale, CA)
    Kelly(R) Science & Clinical is seeking a Regulatory Affairs Process Specialist for a 6-month contract opportunity with a leading molecular diagnostics company ... **Pay rate:** $40-47 per hour. **Company:** Kelly(R) Science & Clinical **Overview and Responsibilities** + The Regulatory ...& Clinical **Overview and Responsibilities** + The Regulatory Affairs Process Specialist will work with the SAP… more
    Kelly Services (07/24/25)
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  • Senior Clinical Research Specialist MDR

    J&J Family of Companies (Irvine, CA)
    …+ Cooperation with the necessary stakeholders ( clinical study team, medical, clinical sites, regulatory , data management) on safety activities related to ... for humanity. Learn more at https://www.jnj.com **Job Function:** Discovery & Pre- Clinical / Clinical Development **Job Sub** **Function:** Clinical more
    J&J Family of Companies (08/29/25)
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  • Program Lead II, Clinical Program…

    AbbVie (San Francisco, CA)
    …programs under consideration. + Reviews and provides clinical operations content to clinical and regulatory documents (eg, INDs, IB, NDAs, BLAs, MAA, ... YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Clinical Operations Program Director is responsible to connect science and… more
    AbbVie (08/13/25)
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  • Director, Global Clinical Compliance (GMP)

    BeOne Medicines (Emeryville, CA)
    …in a relevant field such as Quality Assurance, Supply Chain (commercial and/or clinical ), Manufacturing, Regulatory Compliance, Clinical Development or a ... **General Description:** The Director Global Clinical Compliance builds, collaborates and manages key relations...aptitude to learn about the evolving the legal and regulatory environment, GMP and GDP, applicable laws, regulations and… more
    BeOne Medicines (06/07/25)
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  • Clinical Research Associate, Sponsor…

    IQVIA (Carlsbad, CA)
    …in lieu of degree. * Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. * ie, Good Clinical Practice (GCP) ... in accordance with contracted scope of work and Good Clinical Practice. * Work with sites to adapt, drive,...* Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report… more
    IQVIA (08/13/25)
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  • Clinical Research Coordinator - Neurology

    UCLA Health (Los Angeles, CA)
    …information with judgement and discretion. + Working knowledge of the clinical research regulatory framework and institutional requirements. + Mathematical ... Description The Clinical Research Coordinator contributes to the overall operational...Research Coordinator contributes to the overall operational management of clinical research/trial/study activities from design, set up, conduct, through… more
    UCLA Health (08/29/25)
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  • Clinical Research Coordinator - Surgery

    UCLA Health (Los Angeles, CA)
    …information with judgement and discretion. + Working knowledge of the clinical research regulatory framework and institutional requirements. + Mathematical ... Description The Department of Surgery is seeking to hire a full time Clinical Research Coordinator contributes to the overall operational management of clinical more
    UCLA Health (08/16/25)
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  • Director, Clinical Insights Development

    Abbott (Pleasanton, CA)
    …We have an exciting opportunity for the right candidate to join our Global Clinical and Regulatory Affairs team within the Heart Failure Division (HFD) as ... people in more than 160 countries. **Job Title** **Director, Clinical Insights Development** **Working at Abbott** At Abbott, you...the **Director of Clinical Insights Development.** This role will focus on developing… more
    Abbott (07/21/25)
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  • Clinical Research Specialist II…

    Cedars-Sinai (Los Angeles, CA)
    …**Requirements:** + Bachelor's Degree required. + 5 years of experience in clinical research, regulatory , or data coordination required. + Experience with ... available for this position at this time.** Within ACRO, the Clinical Coordinating Center (CCC) offers infrastructure and expertise for investigator-initiated trials… more
    Cedars-Sinai (06/25/25)
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  • Regulatory Affairs Project Manager

    Abbott (Sylmar, CA)
    …submit applicable reports and ensure appropriate responses are submitted to regulatory authorities + Evaluate proposed preclinical, clinical and manufacturing ... regulatory guidelines, policies and regulations + Ethical guidelines of the regulatory profession, clinical research and regulatory process… more
    Abbott (08/08/25)
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