- 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 and ... ensures studies are complete before being reviewed by the IRB . Manages IRB documents, website, training compliance,...process in a timely manner, ensuring that submissions are review ready prior to routing for review ,… more
- Colorado State University (Fort Collins, CO)
- …documentation of training as regulated federally and by CSU IRB policies. The IRB Coordinator facilitates the research review and approval process of ... Best Towns in America, among other select recognitions:http://www.fcgov.com/fcfacts Position Summary The IRB Coordinator will serve as a contact and resource for… 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, ... all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). **This role is designed to… more
- 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 ... resources, and much more. Posted Job Title Clinical Research Coordinator - A/B (Department of Translational Medicine and Human...regulatory specialist in preparing for all local and Central Institutional Review Board ( IRB… 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 ... are seeking a highly motivated and detail-oriented Clinical Research Coordinator I (CRC I) to support our clinical research...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 ... all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). **What are the Primary Duties… more
- University of Pennsylvania (Philadelphia, PA)
- …data entry. Independently manage different phases of clinical trials. They may assist with Institutional Review Board ( IRB ) filings, sponsor and ... resources, and much more. Posted Job Title Clinical Research Coordinator A/B (Cardiovascular Institute) Job Profile Title Clinical Research...clinical data and data entry. They may assist with 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 ... be a part of breakthrough research?** The Clinical Research Coordinator I works independently providing study coordination, screening of...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 (Beverly Hills, 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 (Beverly Hills, CA)
- …study conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... support a dynamic and collaborative team. The Clinical Research Coordinator I works independently providing study coordination, screening of...including the Food and Drug Administration (FDA) and local 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 ... 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 ... federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). Primary 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 Job Profile Title Clinical Research Coordinator...AEs, SAEs, and UADEs reports to the Investigator and 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 local agencies including the Food and Drug Administration (FDA and local Institutional Review Board . **_*This position is hybrid*_** **Primary Duties… 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 ... in accordance with local and federal guidelines. + May perform other regulatory / Institutional Review Board duties, budgeting duties, and assisting with… more
- Tufts Medicine (Lowell, MA)
- …staff, ensuring protocol adherence, regulatory compliance, data collection, and communication with the Institutional Review Board ( IRB ). Success in this ... reporting any to the (PI), the study sponsor and Institutional Review Board . 8. Reviews... IRB requirements for each study including meeting institutional educational requirements, submitting documents for review ,… 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
- 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)* *Full-time, 40 hours;...protocols, consent forms, and other required documents to the Institutional Review Board ( IRB… 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
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