- HonorHealth (AZ)
- …Summary Coordinates all activities related to the Institutional Review Board and assures compliance with IRB guidelines and FDA regulations. In ... accordance with (45 CFR 46.101-409) the IRB Coordinator facilitates initial and continuing review of...This includes initial determinations regarding expedited, exempt, or full board review , as well as human subject… more
- Vitalief (Livingston, NJ)
- …will support a leading hospital research center in Livingston, NJ, administering and overseeing Institutional Review Board ( IRB ) activities to ensure ... grow sustainably. The Role We are seeking an experienced IRB Coordinator Consultant to join the Vitalief...human subjects research. This role supports investigators, staff, and IRB members in the preparation, review , and… more
- Children's Hospital Los Angeles (Los Angeles, CA)
- …**Schedule:** Day Shift **Purpose Statement/Position Summary:** Protection of human research participants - Institutional Review Board ( IRB ) review ... confirming the regulatory aspects of proposed research for submission to the IRB . The IRB Coordinator II, provides administrative support and coordination to… 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 ... federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). **Primary Duties and… 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 ... all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). **Primary Job Duties and… 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 ... resources, and much more. Posted Job Title Clinical Research Coordinator A/B Job Profile Title Clinical Research Coordinator...responsibilities as assigned CRC-A + Prepare and process all Institutional Review Board ( IRB… more
- University of Miami (Miami, FL)
- …a proven experience in managing regulatory documentation and submissions to entities such as the Institutional Review Board ( IRB ) and the Food and Drug ... has an exciting opportunity for a full-time Clinical Research Coordinator 3 to work in Miami, FL. The Clinical...initial study requests, annual reviews and modifications to the Institutional Review Board ( IRB… more
- Cedars-Sinai (CA)
- …study conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). **Primary Duties &… more
- Cedars-Sinai (Beverly Hills, CA)
- …study conduct. Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... must reside in the commutable area.** The Clinical Research Coordinator II works independently providing study coordination including screening...including the Food and Drug Administration (FDA) and local 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 ... **Job Description** The Clinical Research Coordinator I works independently providing study coordination, screening...including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB… more
- 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 ... gold standard of care we strive for. The Regulatory Coordinator II prepares and submits protocols and supporting documents...including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains… more
- Georgetown Univerisity (Washington, DC)
- …frequent communication with the Institutional Review Board ( IRB ) and compliance offices. The Regulatory Coordinator often serves as the primary ... difference in the world. Requirements Job Overview The Regulatory Coordinator plays a critical role in ensuring regulatory compliance...trial sponsors, Office of Human Subjects Protection, Office of Institutional Review Board and Office… 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 local agencies including the Food and Drug Administration (FDA and local Institutional Review Board . **Primary Duties and Responsibilities:** +… 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 ... Infectious Diseases_** **has an outstanding opportunity open for a** **_Temporary_** **Research Coordinator .** The Research Coordinator primary role is to manage… 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 ... wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator A Job Profile Title Clinical Research Coordinator A Job… 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* *Clinical Research Coordinator - Norwalk, CT* *Full-time: Monday - Friday,...protocols, consent forms, and other required documents to the Institutional Review Board ( IRB… more
- Loyola University Chicago (Chicago, IL)
- …for completion and accuracy with source documents. Prepare regulatory submissions and ensure institutional Review Board renewals are completed. * Assemble ... Clinical Research Coordinator II Thank you for your interest in...assisting in the preparation of initial study documents for IRB submission in compliance with all local, state and… more
- University of Pennsylvania (Philadelphia, PA)
- …duties and responsibilities as assigned Regulatory Responsibilities: + Prepare and process all Institutional Review Board ( IRB ) documentation through the ... programs and resources, and much more. Posted Job Title Clinical Research Coordinator B (Department of Gastroenterology) Job Profile Title Clinical Research … more
- Dialysis Clinic, Inc. (Albany, GA)
- …and post-study closure. They prepare documentation for submission for review by the Institutional Review Board ( IRB ), recruit and screen study ... the collection, preparation, maintenance, and submission of numerous study documents: Institutional Review Board ( IRB ) applications, CV's, medical… more
- Texas A&M University System (Kingsville, TX)
- …University-Kingsville regulations. This includes providing administrative and regulatory oversight for the Institutional Review Board ( IRB ), ... Duties and Responsibilities Regulatory Oversight & Review : + Coordinates the review and processing of research protocols for IRB (human subjects), IACUC… more