- 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
- 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
- UTMB Health (Galveston, TX)
- …regulatory committee reviews of human subjects/animal protocols, including management of Institutional Review Board ( IRB ) committee/ Institutional ... IRB /IACUC Coordinator ( Research , Regulatory,...of protocol review management to assist the Institutional Review Board / Institutional … more
- General Dynamics Information Technology (Portsmouth, VA)
- …Portsmouth (NMCP). The CRC is responsible for providing research coordination support for IRB - and IACUC -approved human and animal research protocols in ... entity may be required for safety reasons. + Coordinate research activities of assigned IRB and IACUC-approved...leadership skills as the coordinator of complex human and animal research protocols. + Maintain… 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 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
- 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 Washington (Seattle, WA)
- …multiple resources available within the University system (eg Grant and Contract Services, Institutional Review Board , Office of Industry Relations) to help ... stroke. This individual will develop and review research tools and protocols, maintain IRB approvals...Prepare interim reports for principal investigators, industry sponsors and Institutional Review Board to ensure… more
- Mount Sinai Health System (New York, NY)
- …study information. Assists in preparing grant applications and documents (for eg, Institutional Review Board , Grants and Contracts Office). ... **Job Description** The Clinical Research Coordinator assists in the daily...research experience Non-Bargaining Unit, 857 - Rehabilitation and Human Performance - ISM, Icahn School of Medicine, Rehab… 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
- 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 Job Profile Title Clinical...of a team, as well as independently; knowledge of IRB and human research protection… more
- Nuvance Health (Danbury, CT)
- … patient, protocol implementation, data collection and query resolution, and submission to the Institutional Review Board ( IRB ). Coordinates studies in ... Prepares and submits all study protocols, consent forms, and other required documents to the Institutional Review Board ( IRB ). * Educates hospital staff… 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