• Clinical Research Data Associate II…

    Cedars-Sinai (Los Angeles, CA)
    …with cancer. **Join our team and contribute to groundbreaking research!** The Clinical Research Data Associate II manages the data for assigned research studies. ... This will include, designing forms for data collection, clinical data abstraction, processing data, maintaining record systems, and producing project reports for… more
    Cedars-Sinai (08/21/25)
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  • EDC/ Clinical Devices Research Coordinator

    US Tech Solutions (South San Francisco, CA)
    …+ The Clinical Research Coordinator, under the oversight of the Clinical Trial Manager and PI, is responsible for independently conducting ... clinical research sessions with study participants. + These sessions...medical device research studies. + Experience maintaining an Electronic Trial Master File (eTMF). **Education:** + BS/BA degree in… more
    US Tech Solutions (07/18/25)
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  • (Senior) Clinical Research Associate…

    IQVIA (Carlsbad, CA)
    …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. *… more
    IQVIA (07/14/25)
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  • Clinical Research Coordinator

    Actalent (Sacramento, CA)
    Job Title: Clinical Research Coordinator Job Description Join a leading medical team as a Clinical Research Coordinator, where you will play a crucial role in ... collection, ordering labs, and overseeing the enrollment and follow-through of oncology trials . Responsibilities + Screen, consent, and enroll patients on oncology … more
    Actalent (09/06/25)
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  • Clinical Data Associate

    University of Southern California (San Diego, CA)
    …development of new treatments for Alzheimer's Disease (AD) through innovative clinical trials . Key Responsibilities: + Data Quality Assessment:Identifying, ... + STEM related bachelor's degree + 1.5 years of experience in clinical trials at a pharmaceutical, biotechnology, or academic clinical research institute… more
    University of Southern California (07/17/25)
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  • Clinical Affairs Manager

    Abbott (Alameda, CA)
    …strategy implementation and operations for overseeing the direction, planning, execution, clinical trials /research and the data collection activities. + ... and negotiates study design and costs. + Responsible for directing human clinical trials , for company products under development. + Participates in adverse event… more
    Abbott (06/27/25)
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  • Clinical Research Associate, Sponsor…

    IQVIA (Carlsbad, CA)
    …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... in accordance with contracted scope of work and Good Clinical Practice. * Work with sites to adapt, drive,...required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's… more
    IQVIA (08/13/25)
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  • Clinical Research Coordinator

    Actalent (Pasadena, CA)
    … Research Coordinator * Administratively and clinically manage an average of six to eight clinical trials * Adhere to Research SOPs * Adhere to Good Clinical ... of FDA, ICH and GCP guidelines. * Experience with Phase I-IV clinical trials * Proficiency with computer programs including Microsoft Office Suite * Excellent… more
    Actalent (09/04/25)
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  • Clinical Research Coordinator II -…

    Cedars-Sinai (Los Angeles, CA)
    …patients with cancer. **Join our team and contribute to groundbreaking research.** The Clinical Research Coordinator II serves as the lead coordinator on an assigned ... regulatory requirements. + Establishes and completes logistical aspects of clinical research projects to achieve project objectives, including project planning,… more
    Cedars-Sinai (08/17/25)
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  • Pathologist

    IQVIA (Valencia, CA)
    …vendors, and employees to achieve shared goals. Act as Principal Investigator on clinical trials and communicate with clients and colleagues on study progress. ... a team. + Provide pathologist input to discussions with clinical trial sponsors to ensure efficient and...daily to meet turnaround times for patient enrollment in clinical trials . + Establish and provide morphological… more
    IQVIA (08/14/25)
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