• CRA / Clinical Site

    Astellas Pharma (Boston, MA)
    …on Astellas, please visit our website at www.astellas.com . **Purpose and Scope:** A Clinical Site Monitor serves as the primary contact point between ... (GCP), and applicable regulations and guidelines from study start-up through to site closure. The Clinical Site Manager will manage the site /sponsor… more
    Astellas Pharma (05/02/25)
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  • Clinical Research Associate

    Insight Global (Franklin Lakes, NJ)
    …that may include devices or drug/device combinations. The Clinical Research Associate serves as a study monitor for moderate to complex studies in ... Job Description Insight Global is looking for a Clinical Research Associate to...as a field-based Clinical Research Associate in the medical device/pharmaceutical industry Strong site more
    Insight Global (06/25/25)
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  • Senior Clinical Research

    BeOne Medicines (San Mateo, CA)
    **General Description:** The SCRA is primarily a site monitor and is responsible for the management and oversight of their assigned clinical study sites to ... with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to manage site ...audit/inspection findings to resolution as it related to involved CRA staff. * Assist with other assigned clinical more
    BeOne Medicines (04/23/25)
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  • Clinical Research Associate

    Cedars-Sinai (Los Angeles, CA)
    …investigation. To learn more, please visit: MIRIAD IBD Biobank & Database | Cedars-Sinai. The Clinical Research Associate I works under the direction of a ... may require on- site training by other experienced clinical research associates. **Qualifications** **Licenses and Certifications:**...the most. **Req ID** : 10829 **Working Title** : Clinical Research Associate I/CPT -… more
    Cedars-Sinai (06/30/25)
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  • Clinical Research Associate

    University of Southern California (San Diego, CA)
    …understanding of study protocol and manuals. + Work closely with Lead Clinical Monitor /Lead CRA to escalate site compliance issues. + Participate in ... Clinical Research AssociateApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/San-Diego-CA/ Clinical - Research - Associate more
    University of Southern California (06/11/25)
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  • Senior Clinical Research

    ICON Clinical Research (TX)
    As a Clinical Research Associate you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare ... site staff training and maintain compliance records + Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting...States without visa sponsorship + A clinical research professional with 2+ years of on- site more
    ICON Clinical Research (07/03/25)
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  • Clinical Research Associate 1

    SUNY Upstate Medical University (Syracuse, NY)
    Job Summary: A Clinical Research Associate I will have a detailed understanding of each study protocol and background knowledge of the study medication and ... patients closely for any associated adverse events. + Maintain clinical research records; maintain files of approval...Interacts with investigators and their staff to facilitate and monitor the conduct of multidepartment clinical studies.… more
    SUNY Upstate Medical University (06/03/25)
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  • Senior Clinical Research

    Edwards Lifesciences (Chicago, IL)
    …Join us and be part of our inspiring journey. We are searching for a **Senior Clinical Research Monitor ** to join Edwards Aortic Field Monitoring team. As a ... Senior Clinical Research Monitor , you ensure...Clinical research certification (ACRP or SOCRA, Clinical Coordinator/ CRA certification) + Prior clinical more
    Edwards Lifesciences (07/02/25)
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  • Senior Clinical Research

    Edwards Lifesciences (San Francisco, CA)
    …us and be part of our inspiring journey. We are searching for a **Senior Clinical Research Monitor ** to join Edwards Transcatheter Pulmonic Field Monitoring ... team. As the Senior Clinical Research Monitor , you will...Clinical Research certification (ACRP or SOCRA, Clinical Coordinator/ CRA certification) Adhere to all company… more
    Edwards Lifesciences (04/23/25)
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  • Clinical Site Lead

    Abbott (Houston, TX)
    …allows for appropriate collaboration with Abbott clinical staff, eg Site CRA , Site Contract Associate . + Train facility staff regarding protocol ... trends, clinical trial enrollment, and ICH-GCP and clinical research application. This individual will adhere... clinical staff (eg, operations management, study team, Site Contracts Associate ), as needed. **Manage all… more
    Abbott (06/05/25)
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  • Clinical Scientist, Early Clinical

    Bristol Myers Squibb (Brisbane, CA)
    …Investigator meetings. + Review clinical narratives. + Collaborate cross-functionally to monitor clinical data for specific trends. + Contribute to the ... meetings as required. + Conduct literature review. + Develop site and CRA training materials and present...preferred). + Expectation of 2+ years of experience in clinical science, clinical research , or… more
    Bristol Myers Squibb (07/04/25)
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  • RN Clinical Research Coordinator

    Novant Health (Winston Salem, NC)
    Research Coordinator IV RN Minimum 1 year* of nursing or clinical research experience required ( CRA , Regulatory, clinic, floor, CRO, ... Job Summary Looking for RNs to join our Clinical Research team! The Clinical...clinical trial related activities. Collects, enters and summarizes clinical trial data. Monitor patients, their results,… more
    Novant Health (06/22/25)
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  • Senior Director Clinical Trials…

    e CancerCare (Fresno, CA)
    …administrator, or physicians. Experience, Qualifications/Education: 3+ years of relevant experience as a clinical research associate or clinical ... the clinic practice site (s). Supervises staff, including Research Nurses, Clinical Research Coordinators,...study budgets with the assistance of the finance department. Monitor all study funds and revenues assuring that sponsor… more
    e CancerCare (05/16/25)
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  • Clinical Research Coordinator

    University of Colorado (Aurora, CO)
    …CCRP - Certified Clinical Research Professional + CCRA - Certified Clinical Research Associate **Knowledge, Skills and Abilities:** + Knowledge and ... ** Clinical Research Coordinator** **Description** **University of...working order + Schedules, coordinates, and prepares for Sponsor Monitor Visits and audits in collaboration with the CCTO… more
    University of Colorado (06/28/25)
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  • Project Manager II, Laboratory

    ICON Clinical Research (Blue Bell, PA)
    …up and responding to clinical study specific inquiries from Sponsors, Physicians, CRA and CRO representatives and the ICON Site Services Department. + Review ... Laboratory ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster...system. Inform team leader about study progress. + Proactively monitor study budget. + Set the timelines for and… more
    ICON Clinical Research (06/27/25)
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  • Sr. Manager, Research Support

    University of Miami (Miami, FL)
    …the following certifications: Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Associate (CCRA), Certified Clinical ... Research Services (CRS) clinical research staff who are assigned to multiple site...Ensures the implementation of training is implemented into daily research procedures. Assess and monitor the implementation… more
    University of Miami (05/03/25)
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  • Regional Director of Radiology

    Baylor Scott & White Health (College Station, TX)
    …injury. Plans and directs programs and activities which may include clinical practice guidance, clinical rotations, utilization, quality, productivity, ... practice and ensures alignment with overall BSWH business aims. Joins with clinical operations, physician leadership, and nursing leadership to drive improvement in… more
    Baylor Scott & White Health (06/07/25)
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