• Cedars Sinai (Los Angeles, CA)
    …federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). Primary Duties and ... and collaborative, multi-site clinical research. The CCC Clinical Research Specialist II will serve in a cross-functional role and...including the Food and Drug Administration (FDA) and local Institutional Review Board . Maintains research… more
    Upward (07/05/25)
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  • Beth Israel Lahey Health (Burlington, MA)
    …the Manager of the Office of Sponsored Research, the Contracts Specialist works with investigators, sponsors and contract research organizations, and collaborating ... research agreements in accordance with Lahey and BILH policies. The Contracts Specialist reviews and negotiates contract terms and conditions, develops and maintains… more
    Upward (07/07/25)
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  • Indiana University (Indianapolis, IN)
    …potential research study subjects; determines eligibility according to the IRB /protocol approved methodologies, coordinates study procedures, and monitors the ... progress of research studies or projects. Conducts study visit activities and coordinates screening, consenting, and scheduling of test, exams, and/or non-medical/behavioral interventions and assessments involving study subjects; coordinates, facilitates, and… more
    Upward (07/15/25)
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  • University of Washington (Seattle, WA)
    …for the department in compliance with UW, federal, and state policies and regulations. - Review proposals for potential IRB , IACUC and SFI issues and work with ... department contacts. Quality Assurance (10%): *Conduct a quality control review of all proposals to ensure each application is...and perform related duties as required. *Liaison to Visa Specialist and VA Contracts Specialist for assigned… more
    Upward (07/25/25)
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  • Cincinnati Children's (Burnet, TX)
    …ethical, regulatory, editorial or content issues before they are submitted for full IRB review . Determine which research protocols or issues have additional ... ethics and guidelines, analyze research protocols submissions (new protocols, continuing review , changes to protocols, one-time use request and adverse events) to… more
    Upward (07/23/25)
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  • Children's Hospital of Philadelphia (Philadelphia, PA)
    …research protocols. What you will do Core responsibilities *Adhere to an IRB approved protocol *Track biospecimens across platforms and performs biospecimen data ... pathology departments and coordinate restocking operations with D3b's supply and shipping specialist *Coordinate transfers and shipments of specimens to and from the… more
    Upward (07/19/25)
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  • Institutional Review Board

    Sanford Health (Sioux Falls, SD)
    IRB is never boring but always rewarding. **Job Summary** The Institutional Review Board ( IRB ) Specialist ensures submitted research is reviewed ... detailed in Sanford Institutional Review Board Policy. Serves in role of IRB ...job (OTJ) training. OTJ training includes two years of Institutional Review Board ( IRB more
    Sanford Health (05/30/25)
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  • Clinical Research Regulatory Specialist

    University of Southern California (Los Angeles, CA)
    …Submits protocols and supporting documents to internal and external regulatory bodies (ie Institutional Review Board ), ensuring trials are consistent with ... and/or operations in the academic or private sector. Experience with submissions to the Institutional Review Board and/or the Federal Drug Administration for… more
    University of Southern California (07/11/25)
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  • Investigator Initiated Trial Specialist

    Stony Brook University (Stony Brook, NY)
    …Investigational New Drug (IND) and Investigational Device Exemption (IDE) applications. + Creating Institutional Review Board ( IRB ) submissions and ... Investigator Initiated Trial Specialist - Clinical Trials **Position Summary** The Cancer...managing correspondence across research sites, particularly in single- IRB /multi-site studies. + Planning and implementing changes to the… more
    Stony Brook University (05/31/25)
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  • Clinical Research Specialist

    University of Maryland, Baltimore (Baltimore, MD)
    …position significantly contributes to the conduct of research. * Coordinates the preparation of Institutional Review Board ( IRB ) and Health Insurance ... Center (UMGCCC) is currently recruiting for a full-time Bone Marrow Research Specialist (Clinical Research Specialist ).* Following an extensive training program,… more
    University of Maryland, Baltimore (07/22/25)
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  • Clinical Research Specialist

    University of Maryland, Baltimore (Baltimore, MD)
    …position significantly contributes to the conduct of research. * Coordinates the preparation of Institutional Review Board ( IRB ) and Health Insurance ... (UMGCCC) has an exciting opportunity for a full-time Clinical Research Specialist for the Hematologic Malignancies research program.*This position will be… more
    University of Maryland, Baltimore (07/22/25)
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  • Clinical Research Specialist II - Clinical…

    Cedars-Sinai (Los Angeles, CA)
    …federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). **Primary Duties and ... and collaborative, multi-site clinical research. The CCC Clinical Research Specialist II will serve in a cross-functional role and...including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains… more
    Cedars-Sinai (06/25/25)
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  • Clinical Research Specialist

    University of Maryland, Baltimore (Baltimore, MD)
    …position significantly contributes to the conduct of research. * Coordinates the preparation of Institutional Review Board ( IRB ) and Health Insurance ... Maryland, Baltimore (UMB) is currently seeking a Clinical Research Specialist .* Accomplishes responsibilities by applying specialized and theoretical knowledge,… more
    University of Maryland, Baltimore (07/10/25)
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  • Sr. Compliance Monitoring Specialist

    Johns Hopkins University (Fort Defiance, AZ)
    …and institutional policies that must be corrected prior to IRB review . + Determine that appropriate protocol and application-specific documentation ... a **_Sr. Compliance Monitoring Specialist_** . There are several Institutional Review Boards (IRBs) that we report...the FDA or commercial sponsors. + Assist in the review of IRB action outcomes, including the… more
    Johns Hopkins University (07/11/25)
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  • Research Nurse Specialist II - Weekend…

    Vanderbilt University Medical Center (Nashville, TN)
    …Research Staff Council monthly meetings. + Attends in-services advertised by the Institutional Review Board , Research Support Services, professional ... prepares and processes new IRB research proposals, amendments, continuing review applications and adverse events according to institutional and departmental… more
    Vanderbilt University Medical Center (07/26/25)
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  • Registered Nurse RN Clinical Research…

    Banner Health (Mesa, AZ)
    …through interactions with research staff, internal and external investigators, study sponsors and Institutional Review Board ( IRB ). 8. Participates in ... last for many years. As a **RN Clinical Research Specialist ** you play a crucial role in clinical trials,...that includes the da Vinci Surgical System. Becker's Hospital Review named Banner Desert Medical Center as one of… more
    Banner Health (07/24/25)
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  • Clinical Study Documentation Specialist

    Caris Life Sciences (Phoenix, AZ)
    …and industry best practices. Responsibilities include maintaining study documentation, coordinating Institutional Review Board ( IRB ) submissions, ... Associates degree + 2 years experience with preparing and submitting documents to Institutional Review Boards (IRBs). + Strong understanding of clinical research… more
    Caris Life Sciences (06/25/25)
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  • Registered Nurse RN Clinical Research…

    Banner Health (Sun City, AZ)
    …through interactions with research staff, internal and external investigators, study sponsors and Institutional Review Board ( IRB ). 8. Participates in ... a safe and ethical manner, while ensuring compliance to the FDA and institutional regulations. **Schedule** : Monday - Friday 8am-5pm, This position will primarily… more
    Banner Health (07/10/25)
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  • Heart Institute Clinical Research Data…

    Cedars-Sinai (Los Angeles, CA)
    …and local agencies, including the Food and Drug Administration (FDA) and local Institutional Review Board . Primary Duties and Responsibilities: + ... to be a part of breakthrough research?** The Clinical Research Data Specialist II independently manages data for assigned research studies, demonstrating a high… more
    Cedars-Sinai (07/10/25)
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  • Program Specialist - Training…

    Kennedy Krieger Institute (Baltimore, MD)
    …bibliography and reference pages, and editing and formatting documents. 14. Assist with Institutional Review Board ( IRB ) applications and renewals, ... **Overview** The Program Specialist I provides day-to-day support to team members throughout the planning, implementation, and delivery of Project ECHO (Extension… more
    Kennedy Krieger Institute (07/25/25)
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