• BioSpace (New York, NY)
    …Organizations (CRO) clinical trial services, with a primary focus on ensuring quality Clinical Research Associate ( CRA ) monitoring and data integrity ... routes. Job Overview: The Clinical Trial Manager (CTM)/ Clinical Research Associate is responsible...Close-Out Visits) to assess CRO's CRA performance, site adherence, and data quality. Monitor key… more
    Upward (07/29/25)
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  • Lifelancer (Andover, MA)
    Site Management and play a pivotal role in shaping the future of global clinical research ! Experienced intermediate level manager in S+N's Global Clinical ... off living. Are you passionate about driving excellence in clinical trials and building strong site relationships...plus 7 or MS plus 5 years' experience in clinical research . Leadership: In addition to above… more
    Upward (07/26/25)
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  • Clinical Site Monitor

    University of Utah (Salt Lake City, UT)
    Details **Open Date** 07/18/2025 **Requisition Number** PRN42572B **Job Title** PS Clinical Site Monitor **Working Title** Clinical Site Monitor ... object to vaccinations. Preferences include credentialing as a Certified Clinical Research Associate ( CCRA...Professional ( CCRP ). Prior experience as an industry CRA or Monitor is also preferred. Hiring… more
    University of Utah (07/18/25)
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  • Clinical Research Associate

    ManpowerGroup (Lake Forest, IL)
    Our client, a leader in the clinical research industry, is seeking a Clinical Research Associate ( CRA ) - B to join their team. As a Clinical ... which will align successfully in the organization. **Job Title:** Clinical Research Associate ( CRA...investigator sites while planning and running study meetings. + Monitor investigational sites to ensure protocol adherence and timely… more
    ManpowerGroup (07/22/25)
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  • Clinical Research Associate

    ConvaTec (VA)
    …Index (LSE:CTEC). To learn more please visit http://www.convatecgroup.com **About the role** The Clinical Research Associate ( CRA ) ensures the effective ... clinical site monitoring across assigned Convatec clinical studies. The CRA assesses clinical...Comprehensive understanding on how to properly assess an investigative site 's capabilities for conducting clinical research more
    ConvaTec (07/25/25)
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  • SR Clinical Research

    Boehringer Ingelheim (Athens, GA)
    **Description** The Senior Clinical Research Associate (SCRA) conducts in-house and external monitoring to verify that reported data collected in Clinical ... of three to five (3-5) years' experience as a CRA / Monitor or similar role. + Good verbal...GLP is a plus. + Certification from a recognized clinical research organization (eg, ACRP or DIA)… more
    Boehringer Ingelheim (07/11/25)
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  • Senior Clinical Research

    BeOne Medicines (Emeryville, 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 (07/23/25)
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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 (07/12/25)
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  • Clinical Research Associate

    ICON Clinical Research (Orlando, FL)
    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 (07/15/25)
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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 (07/15/25)
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  • Sr. Clinical Research

    University of Utah (Salt Lake City, UT)
    …**Job Title** PS Clinical Research Coord Sr. **Working Title** Sr. Clinical Research Associate **Job Grade** F **FLSA Code** Administrative **Patient ... for two years of related work experience); plus, 4 years professional research experience and completion of University RATS Clinical Certification within… more
    University of Utah (07/22/25)
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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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  • Clinical Research Associate

    Trinity Health (Fort Lauderdale, FL)
    …**Description:** Summary This person will be responsible for the conduct of multiple clinical research activities. Ideal candidate will have industry sponsored ... Person is able to work with minimal supervision and within the scope of clinical research protocols, participates in research activities which may include:… more
    Trinity Health (07/19/25)
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  • Clinical Research Monitor

    General Dynamics Information Technology (Fort Detrick, MD)
    …**US Citizenship Required:** Yes **Job Description:** **GDIT's Military Health team is hiring a Clinical Research Monitor to support the Office of Regulated ... Trust/Other Required:** NACLC (T3) **Job Family:** Medical Affairs **Skills:** Clinical Research ,Data Compilation, Research Protocols **Experience:** 4… more
    General Dynamics Information Technology (07/24/25)
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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 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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  • 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 (07/30/25)
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  • Manager, Clinical Research

    Edwards Lifesciences (Sacramento, CA)
    …quality standards + Clinical research certification (ACRP or SOCRA, Clinical Coordinator/ CRA certification) + Prior clinical research experience ... our inspiring journey. We are seeking a **Manager of Clinical Research Monitoring** to join the **Edwards...within parameters of study hypothesis, as well as to monitor clinical trial/study safety, in keeping with… more
    Edwards Lifesciences (07/16/25)
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  • Project Manager II, Laboratory

    ICON Clinical Research (New York, NY)
    …up and responding to clinical study specific inquiries from Sponsors, Physicians, CRA and CRO representatives and the ICON Site Services Department. + Review ... NY 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 (07/29/25)
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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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