• Clinical Research Coordinator

    Kelly Services (Newport Beach, CA)
    …the PI is primarily responsible for the overall conduct of the clinical trial , the CRC manages, supports, facilitates and coordinates the daily clinical trial ... conduct of the study. **Essential Duties and Responsibilities:** + Assisting trial Investigator in screening and reviewing potential study participants eligibility +… more
    Kelly Services (08/16/25)
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  • Clinical Research Coordinator

    System One (Newport Beach, CA)
    …the PI is primarily responsible for the overall conduct of the clinical trial , the CRC manages, supports, facilitates and coordinates the daily clinical trial ... of the study. Essential Duties and Responsibilities: + Assisting trial Investigator in screening and review of potential study...to perform phlebotomy in the state of California is preferred + Excellent verbal & written communication skills +… more
    System One (08/13/25)
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  • Clinical Research Coordinator III - Miriad IBD…

    Cedars-Sinai (Los Angeles, CA)
    …including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent ... including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the… more
    Cedars-Sinai (08/27/25)
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  • Clinical Research Associate ll

    Abbott (Alameda, CA)
    …new study investigators and writing and assembling submissions. + Maintain and audit Trial Master File to ensure inspection readiness. + Perform review of clinical ... of all applicable documents required for the conduct of the study (such as Trial Master File (TMF), Clinical Protocols and Reports). + May interact with RA/QA in… more
    Abbott (08/08/25)
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  • Plaintiff Employment Attorney

    Robert Half Legal (Los Angeles, CA)
    …from intake through resolution - including pleadings, discovery, depositions, mediation, and trial prep. + Draft and argue motions in state and/or federal court. ... + Collaborate with a tight-knit team on case strategy and trial preparation. Qualifications ✅ 3+ years of employment litigation experience (plaintiff-side… more
    Robert Half Legal (07/30/25)
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  • Executive Medical Director, Product Safety…

    BeOne Medicines (Emeryville, CA)
    …Co-ordination training to BeiGene employees on product safety issues and profiles ** Trial Safety** **Support:** + Accountable for safety data, reviews and provides ... Safety Endpoints, safety related inclusion and exclusion criteria data to capture during trial , key review activities and timing, reviews and leads input on product… more
    BeOne Medicines (07/25/25)
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  • Senior Director, Metrics, Analytics & Insights,…

    BeOne Medicines (San Mateo, CA)
    …and metrics. The objective is to provide transparency into clinical trial execution, improve operational efficiency, optimize resource utilization, and ensure ... to support strategic initiatives and business-critical reporting needs across global clinical trial operations. The Senior Director is expected to: + Develop and… more
    BeOne Medicines (07/17/25)
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  • Associate Attorney

    Robert Half Legal (San Diego, CA)
    …focusing on witness depositions and discovery-heavy tasks. * Collaborate with partners on trial preparation and attend trials as part of the litigation team. * Draft ... * Provide hands-on support throughout the litigation process, from intake to trial . * Maintain accurate and detail-oriented billing practices, adhering to firm… more
    Robert Half Legal (07/12/25)
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  • Litigation Associate

    Robert Half Legal (Los Angeles, CA)
    …- taking and defending o Drafting legal documents - complaints and motions o Preparing for trial - do trial experience required, but firm does go to trial ... complex matters . Associates get to help prepare for trial - draft exhibit books, cross examine witnesses, even...in CA - probate, business, or real estate litigation preferred + ABA-accredited law school, top 100 ideally +… more
    Robert Half Legal (07/08/25)
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  • Senior Clinical Scientist - Job ID: SCS

    Ascendis Pharma (Palo Alto, CA)
    …retention + Ensure successful completion of documents (including clinical trial protocols, investigator brochures, monitoring plans, site training materials, ... and efficacy data + Anticipate obstacles within a clinical trial , and implement solutions + Analyze, evaluate, and support...information + Lead both directly and by example + Preferred , but not required: + At least 4 years… more
    Ascendis Pharma (07/04/25)
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