• (Senior) Clinical Research

    IQVIA (Durham, NC)
    …in lieu of degree. * In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, ie, Good Clinical Practice (GCP) and ... with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… more
    IQVIA (10/17/24)
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  • Clinical Research Associate

    IQVIA (San Diego, CA)
    **Job Overview** Join our team as a Clinical Research Site Manager, where you'll play a crucial role in ensuring our study sites operate seamlessly and adhere to ... all protocols, regulations, and sponsor requirements. **Essential Functions** + **Site Monitoring:** Conduct selection,...and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
    IQVIA (09/14/24)
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  • Clinical Research Associate

    IQVIA (Parsippany, NJ)
    …and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. You should have: + A Bachelor's degree ... or at least three months of on-site monitoring experience. 2 years of clinical research coordinator experience strongly preferred. + Alternatively, you should… more
    IQVIA (09/06/24)
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  • Clinical Data Coordinator I - Hybrid

    Caris Life Sciences (Boston, MA)
    …Communicate effectively with the research team, investigator(s), Clinical Research Associate (s), study sponsor and ancillary staff. **Required ... case report forms and other information related to data collection for clinical research . Must respond to queries in a timely fashion. Schedule on-site visits… more
    Caris Life Sciences (10/03/24)
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  • Clinical Research Data Specialist II

    University of Southern California (Los Angeles, CA)
    …or Study Coordinator of issues or violations. + Acts as primary site contact with sponsor 's Clinical Research Associate (CRA) for externally sponsored ... Clinical Research Data Specialist IIApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ Clinical -… more
    University of Southern California (09/17/24)
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  • Research Team Clinical Data…

    ThermoFisher Scientific (Las Vegas, NV)
    …the successful completion and filing of case report forms and source documents for clinical research studies. Works with sponsor representatives at all ... safety and positive impact on patient's lives. As a Research Team Clinical Data Associate ,...accurate and timely completion of study CRFs to meet sponsor requirements and deadlines. Informs Research Team… more
    ThermoFisher Scientific (11/16/24)
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  • Clinical Research Associate

    Mount Sinai Health System (New York, NY)
    **Job Description** The Clinical Research Associate is an integral part of the research study team and monitors all safety aspects of clinical ... studies as a clinical trial assistant or clinical research associate is required....all study related correspondence with the investigative sites and sponsor including, but not limited to associated correspondence, CEC… more
    Mount Sinai Health System (10/23/24)
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  • CRA II or Senior CRA, Single- Sponsor

    ICON Clinical Research (Los Angeles, CA)
    …friendliest people in the sector, and you'll be helping shape an industry. As a Clinical Research Associate at ICON, you'll work within a large-scale, ... CRA II or Senior CRA (Single- Sponsor ) ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an… more
    ICON Clinical Research (10/24/24)
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  • Associate Clinical Research

    Rush University Medical Center (Chicago, IL)
    …**Shift 1** **Work Schedule:** 8 Hr (8:00:00 AM - 4:30:00 PM) **Summary:** The Associate Clinical Research Coordinator is a highly organized individual who ... disability, veteran status, and other legally protected characteristics.** **Position** Associate Clinical Research Coordinator **Location** US:IL:Chicago… more
    Rush University Medical Center (09/20/24)
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  • Sr. CRA, Sponsor Aligned, Oncology

    IQVIA (Carlsbad, CA)
    Job Overview: Join our dynamic team as a Clinical Research Associate ! You'll play a pivotal role in monitoring and managing clinical trial sites to ... ensure compliance with study protocols, regulations, and sponsor requirements. Be at the forefront of groundbreaking...from you! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
    IQVIA (10/03/24)
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  • Clin Research Associate

    Hartford HealthCare (Bridgeport, CT)
    …to us. *Job Summary:* As a specialized research professional the Senior Clinical Research Associate (SrCRA) collaborates with the Principal Investigator ... these duties, the SrCRA works with the PI, department, sponsor , IRB and institution to support and provide guidance...all aspects of study activity as required of a Clinical Research Associate This is… more
    Hartford HealthCare (11/01/24)
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  • Sr. Clinical Research

    J&J Family of Companies (Danvers, MA)
    …Learn more at https://www.jnj.com/. Johnson & Johnson Medtech is recruiting for a Sr Clinical Research Associate , located anywhere in the United States. For ... site activities on assigned clinical trials. The Clinical Research Associate should ensure...+ Conduct site initiation visits; train site personnel on sponsor and regulatory requirements for study conduct; participate in… more
    J&J Family of Companies (11/14/24)
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  • Clinical Research Associate

    Cedars-Sinai (Los Angeles, CA)
    …your experience with an organization known nationally for excellence in research !** The Clinical Research Associate I/CPT works under the direction of a ... for external sponsors for select trials. May respond to sponsor inquiries and attend meetings regarding study activity under...job functions. **Req ID** : 6144 **Working Title** : Clinical Research Associate I/CPT, Heart… more
    Cedars-Sinai (11/14/24)
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  • Clinical Research Associate

    Cedars-Sinai (Los Angeles, CA)
    …pulses through Cedars-Sinai. **We invite you to consider this phenomenal opportunity!** As a Clinical Research Associate I, you will work directly with a ... external sponsors for select trials. + May respond to sponsor inquiries and attend meetings regarding study activity under...the most. **Req ID** : 6385 **Working Title** : Clinical Research Associate I -… more
    Cedars-Sinai (11/14/24)
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  • Clinical Research Coordinator…

    Stanford University (Stanford, CA)
    Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United States** Research Post Date Dec 08, 2023 Requisition # 101673 ... Stanford University's Department of Neurosurgery is seeking a Clinical Research Coordinator Associate (CRCA)...**Duties Include*:** + Serve as the primary contact with research participants, sponsor , and regulatory agencies. +… more
    Stanford University (09/05/24)
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  • Clinical Research Coordinator…

    Stanford University (Stanford, CA)
    Clinical Research Coordinator Associate , Stanford Child Wellness Lab **Stanford, California, United States** **New** Research Post Date 3 days ago ... Care Medicine is seeking aClinical Research Coordinator Associate to conduct clinical research ...understanding and adhering to compliance regulations from IRB, FDA, Sponsor , etc.Participate in monitor visits and regulatory audits. +… more
    Stanford University (11/15/24)
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  • Senior Associate Sponsored Research

    Emory Healthcare/Emory University (Atlanta, GA)
    …**Description** JOB DESCRIPTION: ** This position is located in the Office of Research -Woodruff Industry Sponsored Clinical Trials department. ** + Provides ... **Discover Your Career at Emory University** Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate… more
    Emory Healthcare/Emory University (10/17/24)
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  • Clinical Research Associate

    Cordis (Irvine, CA)
    …place for you. Join us, and let's improve the wellbeing of millions, together. The Clinical Research Associate (CRA) reports to the Clinical Monitoring ... documentation is available in the site's investigator file and sponsor trial master file + Support clinical ...+ A minimum of 5 years' experience as a clinical research associate preferred with… more
    Cordis (11/13/24)
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  • Senior Clinical Research

    Danaher Corporation (Chaska, MN)
    …with diagnostic tools that address the world's biggest health challenges. The Senior Clinical Research Associate for Beckman Coulter Diagnostics is ... communicate with internal and external stakeholders who possess various levels of clinical research experience. + Ability to independently complete IRB… more
    Danaher Corporation (09/06/24)
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  • Clinical Research Associate 1

    SUNY Upstate Medical University (Syracuse, NY)
    Job Summary: Coordination of clinical research studies. Performance of regulatory tasks including IRB and sponsor /CRO regulatory correspondence. ... Data collection and entry into paper and electronic databases. Maintenance of clinical research supply inventory. Processing clinical trial billing… more
    SUNY Upstate Medical University (10/21/24)
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