- 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
- Virtua Health (Marlton, NJ)
- …Supports the IRB by triaging and managing submissions through a pre- review process for completeness. Supports the research community by providing policy ... a related field. May substitute required education with related human subjects protection and/or research administrative experience...a two to one basis Training / Licensure: Human Subjects Protection training. Certified IRB Professional… more
- HonorHealth (AZ)
- …Summary Coordinates all activities related to the Institutional Review Board and assures compliance with IRB guidelines and FDA regulations. In ... IRB Coordinator facilitates initial and continuing review of research protocols in compliance with...This includes initial determinations regarding expedited, exempt, or full board review , as well as human… 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
- University of Rochester (Rochester, NY)
- …the individual, and internal equity considerations._ **Responsibilities:** GENERAL SUMMARY The Human Subject Coordinator (HSRC) Trainee will assist with ... the Adolescent Brain and Cognitive Development (ABCD) Study, a federally funded research study in the Cognitive Neurophysiology Lab. General protocol and directions… more
- University of Rochester (Rochester, NY)
- …equity considerations._ **Responsibilities:** GENERAL SUMMARY We are in search of a human subject research specialist to help support and evaluate community-led ... + Becomes proficient in the development and/or update of IRB protocols to evaluate new initiatives + Assists in...supervision of PI. + Maintains eligibility to participate in research involving human subjects including completing all… more
- University of Colorado (Aurora, CO)
- …Office of Regulatory Compliance - Colorado Multiple Institutional Review Board ** **Job Title: IRB Panel Coordinator ** **Position #:00696471 - ... Review Boards or OHRP/FDA regulations regarding human subject research + Certified IRB...the Colorado Multiple Institutional Review Board (COMIRB) conducts reviews of submitted human … 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
- 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 to...Associate's degree and completion of 6 months in the Human Subject Research Coordinator Trainee… more
- MetroHealth (Cleveland, OH)
- … coordinator working with human subjects. Experience working with an Institutional Review Board ( IRB ). Good organizational and problem-solving ... or other related field. Three years of experience working as a clinical research coordinator working with human subjects, or two years of experience and… 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 Washington (Seattle, WA)
- …media. The coordinator will oversee research billing compliance, maintain Institutional Review Board documents, modifications, and status reports. A ... coordinator will be responsible for drafting and maintaining Institutional Review Board documents, modifications,...samples and blood) in accordance with established protocols. The research coordinator will track available human… more
- University of Rochester (Rochester, NY)
- …met before enrollment. + 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 to...Associate's degree and completion of 6 months in the Human Subject Research Coordinator Trainee… 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...AEs, SAEs, and UADEs reports to the Investigator and Institutional Review Board ( IRB… more
- Nuvance Health (Danbury, CT)
- … patient, protocol implementation, data collection and query resolution, and submission to the Institutional Review Board ( IRB ). Coordinates studies in ... *Description* *Clinical Research Coordinator - Danbury Hospital (On-site)*...protocols, consent forms, and other required documents to the Institutional Review Board ( IRB… more
- University of Washington (Seattle, WA)
- …procedures, recruitment, monitoring study progress, data analysis, and work with the UW institutional review board . Current projects include an NIH-funded ... Diseases_** **has an outstanding opportunity open for a** **_Temporary_** ** Research Coordinator .** The Research ...* Research specific training in Protection of Human Research Subjects. * Self-starter and able… more
- Nuvance Health (Norwalk, CT)
- … patient, protocol implementation, data collection and query resolution, and submission to the Institutional Review Board ( IRB ). Coordinates studies in ... *Description* *Title: *Clinical Research Coordinator **- Norwalk Hospital Cancer ...protocols, consent forms, and other required documents to the Institutional Review Board ( IRB… 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
- HCA Healthcare (Kansas City, MO)
- …Functions as a liaison between investigators, subjects, sponsors, the Institution, and the Institutional Review Board ( IRB ). **What you will ... our team. **Job Summary and Qualifications** The Trauma Clinical Research Coordinator will coordinate and participate in...literature and regulatory reviews. + Prepares reports for the Institutional Review Board . Ensures completeness… more
- Stanford University (Stanford, CA)
- …for completion and accuracy with source documents. Prepare regulatory submissions and ensure institutional Review Board renewals are completed. + Assemble ... Clinical Research Coordinator Associate **School of Medicine,...IRB . Protect the rights, safety and well-being of human subjects involved in the clinical trials. **Duties include*:**… more