- University of Rochester (Rochester, NY)
- …degree Required + OR Associate's degree and completion of 6 months in the Human Subject Research Coordinator Trainee Program Required + Or equivalent ... compliance, and queries. + Assists with specimen processing and shipping. + Serves as back-up research coordinator in the absence of the HSRC II. Serves as the… more
- Johns Hopkins University (Baltimore, MD)
- …part of a team that processes human subjects research protocols overseen by the Institutional Review Board ( IRB ). The IRB Coordinator is ... to document the IRB 's decision regarding the review of human subjects research ...extent permitted by the JHU equivalency formula. Classified Title: IRB Coordinator Role/Level/Range: ATO 37.5/03/OF Starting Salary… more
- Mount Sinai Health System (New York, NY)
- …in the preparation and submission of grant applications and documents (eg, Institutional Review Board , Grants and Contracts Office). **Qualifications** ... **Job Description** The Clinical Research Coordinator is an entry human subjects...telephone calls. + Assists in the collection, analysis and review of experimental data for publication and presentation. +… more
- University of Rochester (Rochester, NY)
- …interventional activities, to document adverse events and report to senior study staff, PI, Institutional Review Board ( IRB ), Sponsor, and/or any other ... internal equity considerations._ **Responsibilities:** Coordinates the activities associated with human subject research . RESPONSIBILITIES: - Coordinates the… more
- Vitalief (Livingston, NJ)
- …a leading hospital research center in Livingston, NJ, administering and overseeing Institutional Review Board ( IRB ) activities to ensure compliance ... institutional regulations governing human subjects research . This role supports investigators, staff, and IRB... research . This role supports investigators, staff, and IRB members in the preparation, review , and… more
- University of Colorado (Aurora, CO)
- …working with Institutional Review Boards or OHRP/FDA regulations regarding human subject research . + Certified IRB Manager (CIM) or Certified ... **University of Colorado Anschutz Medical Campus** **Department: Colorado Multiple Institutional Review Board - Office...diversity and inclusion. + Working knowledge of Office for Human Research Protections (OHRP) and Food and… more
- University of Rochester (Rochester, NY)
- …interventional activities, to document adverse events and report to senior study staff, PI, Institutional Review Board ( IRB ), Sponsor, and/or any other ... forms and CRFs, are complete, accurate, and available for review . + Communicates with Sponsor to clarify data queries...Associate's degree and completion of 6 months in the Human Subject Research Coordinator Trainee… more
- University of Rochester (Rochester, NY)
- …+ Bachelor's degree or Associate's degree and completion of 6 months in the Human Subject Research Coordinator Trainee Program + Or an equivalent ... of the individual, and internal equity considerations._ **Responsibilities:** GENERAL PURPOSE The Human Subject Research Specialist I (HSRS I) plays a vital… more
- University of Colorado (Aurora, CO)
- …in an academic medical research environment + Experience submitting protocols to an institutional review board ( IRB ) + REDCap development and ... preparation and submission (locally and to DOD Office of Human Research Protections, as well as coordinating...structured process improvement methods; and experience developing and submitting institutional review board protocols for… more
- University of Pennsylvania (Philadelphia, PA)
- …biological samples and related study documents, and collection of clinical data. Assist with Institutional Review Board ( IRB ) filings and inquiries, and ... and resources, and much more. Posted Job Title Clinical Research Coordinator A/B Job Profile Title Clinical...responsibilities as assigned CRC-A + Prepare and process all Institutional Review Board ( IRB… more
- University of Southern California (Los Angeles, CA)
- … is performed as described in protocol. Serves as contact for subjects, study personnel, Institutional Review Board ( IRB ) and study sponsor. + Assists ... Medicine at Keck School of Medicine is seeking a Research Coordinator . Working directly under the supervision...study continuing review and study amendments to Institutional Review Board ( IRB… more
- Cedars-Sinai (Los Angeles, CA)
- …study conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... and the greatest needs in our region. The Clinical Research Coordinator II works independently providing study...including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB… more
- Stanford University (Stanford, CA)
- …bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices. IRB submissions. + 2-4 years ... Clinical Research Coordinator 2 **School of Medicine,...provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and… more
- University of Washington (Seattle, WA)
- …and quantitative research and data collection + Experience developing and submitting Institutional Review Board ( IRB ) proposal and modification ... of General Internal Medicine (GIM)** **has an outstanding opportunity for a** ** Research Coordinator 2** **PostingTitle** **to join their team.** The University… more
- University of Washington (Seattle, WA)
- …writing IRB applications/modifications for complex research protocols. + Maintain Institutional Review Board ( IRB ) approvals and correspondence, ... Emergency Medicine_** **has an outstanding opportunity for a** **_Temporary_** ** Research Coordinator ** **to participate in clinical ...sharing. + Prepare and maintain study materials for the Institutional Review Board ( IRB… more
- Stanford University (Stanford, CA)
- …procedures and reporting. + Demonstrated experience with regulatory requirements including Institutional Review Board requirements, HIPAA, and Good ... protocols and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices.… more
- Mount Sinai Health System (New York, NY)
- …organizes study information. Assists in preparing grant applications and documents (for eg, Institutional Review Board , Grants and Contracts Office). We are ... **Job Description** The Clinical Research Coordinator assists in the daily...well as part of a team. + Familiarity with IRB processes, research ethics, and HIPAA compliance… more
- University of Pennsylvania (Philadelphia, PA)
- … visits in clinic; maintaining regulatory files; and preparing submissions to the Penn Biomedical Institutional Review Board ( IRB ) and central IRBs when ... and resources, and much more. Posted Job Title Clinical Research Coordinator B Job Profile Title Clinical...of a team, as well as independently; knowledge of IRB and human research protection… more
- Texas A&M University System (Kingsville, TX)
- …University-Kingsville regulations. This includes providing administrative and regulatory oversight for the Institutional Review Board ( IRB ), ... + Coordinates the review and processing of research protocols for IRB ( human ...institutional policies. Export Control Compliance: + Assists with review of research activities for restrictions, technology… more
- Dartmouth Health (Lebanon, NH)
- …standards operating procedures for the execution of clinical trial operations, including timely Institutional Review Board ( IRB ) submissions meeting ... Overview Clinical Research Coordinator I works closely with...with regulatory processes. * Maintains basic current understanding of IRB and Dartmouth-Hitchcock Health (D-HH) Institutional processes.… more