- 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
- BayCare Health System (Clearwater, FL)
- …**Facility:** BayCare Systems Office (Hybrid) **Responsibilities:** + Provide functional support to the Institutional Review Board ( IRB ). + Responsible ... - 5:00PM **Weekend Work:** None **Equal Opportunity Employer Veterans/Disabled** **Position** IRB Coordinator **Location** Clearwater:BayCare Sys Office West |… more
- University of Colorado (Aurora, CO)
- …** **Description** **University of Colorado Anschutz Medical Campus** **Department: Colorado Multiple Institutional Review Board - Office of Regulatory ... a year for year basis. **Preferred Qualifications:** + Experience working with Institutional Review Boards or OHRP/FDA regulations regarding human subject… more
- UTMB Health (Galveston, TX)
- …Coordinates regulatory committee reviews of human subjects/animal protocols, including management of Institutional Review Board ( IRB ) committee/ ... IRB /IACUC Coordinator (Research, Regulatory, & Compliance...of protocol review management to assist the Institutional Review Board / Institutional … 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
- 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 II works independently providing study coordination including...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 II works independently providing study coordination including...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)
- …study conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... you be doing in this role?** 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
- 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 (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)
- …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
- University of Southern California (Los Angeles, CA)
- …research is performed as described in protocol. Serves as contact for subjects, study personnel, Institutional Review Board ( IRB ) and study sponsor. + ... at Keck School of Medicine is seeking a Research Coordinator . Working directly under the supervision of Dr. Linda...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 ... the greatest needs in our region. 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
- 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, Stanford, California, United...provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and… 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 Pennsylvania (Philadelphia, PA)
- …visits in clinic; maintaining regulatory files; and preparing submissions to the Penn Biomedical Institutional Review Board ( IRB ) and central IRBs when ... e-regulatory binders and required tracking logs. Assemble and submit documents to institutional committees for study activation (eg, IRB , CTSRMC), ensuring… more
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