• IRB Review Specialist

    University of Colorado (Aurora, CO)
    …**University of Colorado Anschutz Medical Campus** **Department: Colorado Multiple Institutional Review Board (COMIRB)** **Job Title: IRB Review ... ** IRB Review Specialist ** **Description**...of 1 days per week on campus The Colorado Multiple Institutional Review Board (COMIRB) exists to … more
    University of Colorado (10/31/24)
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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 ... them through procedures and visits required by the research protocol . The Bone Marrow Research Specialist is...Serves as a liaison to other departments such as IRB or CCT, outside organizations, government agencies, and product… more
    University of Maryland, Baltimore (11/07/24)
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  • Clinical Research Senior Assistant or Clinical…

    University of Maryland, Baltimore (Baltimore, MD)
    …collection and clarification, and general administrative duties. * Assists in the preparation of Institutional Review Board ( IRB ) and Health Insurance ... them through procedures and visits required by the research protocol . The Bone Marrow Clinical Research Senior Assistant/ Specialist...the conduct of research. * Coordinates the preparation of Institutional Review Board ( IRB more
    University of Maryland, Baltimore (09/24/24)
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  • Research Nurse Specialist - Cancer

    Northwell Health (Lake Success, NY)
    …adherence to established protocols to ensure projects are carried out as directed by the Institutional Review Board ( IRB ). Works within scope of practice ... Drug Administration (FDA), Good Clinical Practice, institutional policies, sponsor requirements, Institutional Review Board ( IRB ) and related… more
    Northwell Health (10/30/24)
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  • Regulatory Specialist II

    AdventHealth (Orlando, FL)
    …setting, with at least 2 years in a clinical research setting including an institutional review board office, research administration, or regulatory affairs ... Specialist II functions as a liaison between the IRB of record for each study protocol ,...review , approval, and clearance activities for each research protocol maintaining detailed, complete, accurate and current records at… more
    AdventHealth (11/01/24)
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  • Senior Regulatory Compliance Specialist

    Houston Methodist (Houston, TX)
    …laws, regulations, guidance, policy and procedure developed by Houston Methodist Research Institute Institutional Review Board ( IRB ), Food and Drug ... forms and associated documentation + Serves as a liaison between the institutional review committees, regulatory agencies, and the investigators to ensure… more
    Houston Methodist (10/09/24)
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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 (10/29/24)
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  • Regulatory Specialist

    Actalent (Hackensack, NJ)
    …serve as a liaison to investigators, collaborating divisions, departments, and institutions, the Institutional Review Board ( IRB ), and external ... Job Title: Regulatory Specialist Job Description The Regulatory Specialist ...Serious Adverse Event (SAE) and IND safety reports. - Review and interpret IRB correspondence with the… more
    Actalent (11/05/24)
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  • Regulatory Specialist

    Actalent (Hackensack, NJ)
    …serve as a liaison to investigators, collaborating divisions, departments and institutions, the Institutional Review Board ( IRB ), and external regulatory ... Job Title: Regulatory Specialist Job Description The Regulatory Specialist ...Serious Adverse Event (SAE) and IND safety reports. + Review and interpret IRB correspondence with the… more
    Actalent (11/05/24)
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  • Human Research Protection Specialist

    Magellan Health Services (Falls Church, VA)
    …subject matter expert to Institutional Officials, Human Research Protections Officers (HRPOs), Institutional Review Board ( IRB ) members and staff, ... will assist with oversight of human research protection programs, Institutional Review Boards (IRBs), human subject protection...a final Assessment report or summary. + Headquarters Level Review of IRB reviewed protocols for which… more
    Magellan Health Services (10/30/24)
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  • Regulatory Specialist

    Weill Cornell Medical College (New York, NY)
    …and submits all necessary documents to the Clinical Science Evaluation Committee (CSEC), the Institutional Review Board ( IRB ) and ancillary committees. + ... Title: Regulatory Specialist Location: Upper East Side Org Unit: Geriatrics...+ Reports all Serious Adverse Events (SAEs) to the Institutional Review Board and other… more
    Weill Cornell Medical College (10/19/24)
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  • Specialist , Clinical Research

    University of Maryland, Baltimore (Baltimore, MD)
    …significantly contributes to the conduct of research. * Coordinates the preparation of the Institutional Review Board ( IRB ) and Health Insurance ... and Translational Research (ICTR)*is currently recruiting for a*Clinical Research Specialist *. This position is responsible for overseeing and coordinating the… more
    University of Maryland, Baltimore (11/08/24)
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  • Clinical Research Specialist I - Heart…

    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 ... known nationally for excellence in research!** The Clinical Research Specialist I provides clinical research expertise by participating in...including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains… more
    Cedars-Sinai (10/23/24)
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  • Clinical Research Specialist

    Dignity Health (Phoenix, AZ)
    …Administration (FDA) Office for Human Research Protections (OHRP) Good Clinical Practices (GCP) Institutional Review Board ( IRB ) HIPAA regulations and ... limited to the following duties: + Knowledge of regulatory requirements and institutional requirements when conducting study protocol (s). + Assists with… more
    Dignity Health (10/31/24)
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  • Clinical Research Coordinator - A/B (Department…

    University of Pennsylvania (Philadelphia, PA)
    …B will assist the regulatory specialist in preparing for all local and Central Institutional Review Board ( IRB ) documentation through the IRB , ... Williams Syndrome. Clinical Research Coordinator work includes study design, protocol development, submission to review boards, subject...specialist in preparing for all local and Central Institutional Review Board ( IRB more
    University of Pennsylvania (10/27/24)
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  • Regulatory Specialist - CRI

    Methodist Health System (Dallas, TX)
    …the IRB . * Create and/or adapt clinical trial informed consent documents for Institutional Review Board ( IRB ) submission. * Maintain regulatory ... Shift :** **Job Description :** Your Job: The Regulatory Specialist will perform expertise in the regulatory component of...events in accordance with Food and Drug Administration, sponsor protocol , and IRB regulations and guidelines. *… more
    Methodist Health System (10/12/24)
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  • Regulatory Specialist

    Hackensack Meridian Health (Paramus, NJ)
    …and external investigators, sponsors, collaborating divisions, departments and institutions, and Institutional Review Boards (IRBs), Data Safety and Monitoring ... for a clinical trial in order to initiate a review in tandem with IRB review...documents pertaining to the DSMB, Biosafety Committee, and the Protocol Review Committee, when applicable. + Arranges… more
    Hackensack Meridian Health (09/28/24)
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  • Quality Assurance and Data Management…

    Pennsylvania State University (University Park, PA)
    …In this dynamic position, the successful candidate will monitor and audit IRB protocol compliance, assist with the management of ClinicalTrials.gov accounts, ... and state regulations, track audit outcomes, and handle self-assessment audits to ensure IRB protocol adherence. + FDA QA Support: Offer support for… more
    Pennsylvania State University (10/12/24)
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  • Regulatory Affairs Specialist

    Dana-Farber Cancer Institute (Boston, MA)
    …and review of select protocol and monitoring processes prior to IRB review . The Regulatory Affairs Specialist (RAS) positions are critical to ... The Regulatory Affairs Specialist (RAS) positions provides advanced expertise and regulatory... protocol documents in order to ensure timely scientific/ IRB review and approval. + Evaluates research… more
    Dana-Farber Cancer Institute (09/07/24)
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  • Research Compliance Specialist Senior

    Highmark Health (Pittsburgh, PA)
    …RESPONSIBILITIES:** + Manages work flow processes and conducts activities pertaining to IRB review and approval for protocols involving human subjects submitted ... OVERVIEW:** Ensures compliance with federal regulations, state laws and institutional guidelines throughout the review and approval...by researchers; monitors the protocol review process to ensure complete and… more
    Highmark Health (11/04/24)
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