• Clinical Review Specialist II (On-Site)

    UCLA Health (Santa Monica, CA)
    …outcomes for the communities we serve. You will also facilitate compliance with clinical quality regulatory requirements while promoting a culture of safety. ... for the identification, collection, and entry of quality data for the Clinical Registries, Patient Safety Indicators (PSIs), and Hospital Acquired Conditions (HACs)… more
    UCLA Health (08/26/25)
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  • Sr. Clinical Research Training Specialist

    Children's Hospital Los Angeles (Los Angeles, CA)
    …experiences, perspectives and backgrounds allow us to better serve our patients and create a strong community at CHLA. Clinical Research Regulatory Affairs ... care that is personal, convenient and empowering. Our scientists will work with clinical experts to take laboratory discoveries and create treatments that are a… more
    Children's Hospital Los Angeles (08/28/25)
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  • Associate Director Regulatory Affairs

    Abbott (San Diego, CA)
    …Recruit, develop, and mentor regulatory professionals. **Premarket:** + Approve regulatory filing strategies based on proposed preclinical, clinical , and ... regulatory guidelines, policies and regulations Ethical guidelines of the regulatory profession, clinical research and regulatory process. **Preferred… more
    Abbott (07/10/25)
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  • Regulatory Affairs Specialist III

    Kelly Services (San Fernando, CA)
    ** Regulatory Affairs Specialist III - San Fernando, CA** Kelly(R) Science & Clinical is seeking a ** Regulatory Affairs Specialist III** for a full-time ... and ready to take the next step in your regulatory career, let your expertise shape the future with...the Kelly Talent Community. Why Kelly (R) Science & Clinical ? Kelly Science & Clinical is your… more
    Kelly Services (08/21/25)
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  • Regulatory Affairs Manager

    Kelly Services (Valencia, CA)
    …$100,000-$140,000/year (DOE) + **Industry:** Medical Device / Life Sciences Kelly(R) Science & Clinical is hiring a ** Regulatory Affairs Manager** for a leading ... + ** Regulatory Affairs Manager** + **Location:** Onsite in Valencia...of future opportunities in the field of science and clinical research. **Join us in making a difference by… more
    Kelly Services (08/16/25)
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  • Regulatory Affairs Manager - Heart Failure…

    Abbott (Pleasanton, CA)
    regulatory guidelines, policies and regulations + Ethical guidelines of the regulatory profession, clinical research and regulatory process ... mothers, female executives, and scientists **The Opportunity** We are seeking a ** Regulatory Affairs Manager** to join Abbott's Heart Failure Division on-site in… more
    Abbott (06/16/25)
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  • Clinical Development Program Lead,…

    Bristol Myers Squibb (San Diego, CA)
    …of clinical trials and will supervise and have accountability for the clinical components of regulatory filings + Will contribute to overall strategy for ... a clinical development leader; with greater than 10 years of extensive clinical trial, drug development, and regulatory experience, in addition to a strong… more
    Bristol Myers Squibb (08/20/25)
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  • Director, Clinical Development (MD)

    Gilead Sciences, Inc. (Foster City, CA)
    …portfolio. This individual will play a key role in shaping clinical strategy, collaborating cross-functionally with research, regulatory , safety, and ... trial protocols for inflammation programs, ensuring scientific rigor and regulatory compliance. + Serve as the clinical ...and regulatory compliance. + Serve as the clinical lead on cross-functional study teams, providing medical and… more
    Gilead Sciences, Inc. (08/02/25)
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  • Director II, Clinical Development

    AbbVie (Irvine, CA)
    …interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses and other ... regulatory requirements related to botulinum toxin and aesthetic clinical studies and global drug development, exemplifying compliance with those requirements.… more
    AbbVie (07/22/25)
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  • Senior Scientific Director, Clinical

    AbbVie (Irvine, CA)
    …interpretation and reporting of scientific content of protocols, Investigator Brochures, Clinical Study reports, regulatory submissions and responses and other ... area. May represent AbbVie at key external meetings. *Responsible for understanding the regulatory requirements related to the clinical studies and global drug… more
    AbbVie (08/08/25)
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