- Texas A&M University System (Kingsville, TX)
- …University-Kingsville regulations. This includes providing administrative and regulatory oversight for the Institutional Review Board ( IRB ), ... Job Title Research Compliance Coordinator Agency...+ Coordinates the review and processing of research protocols for IRB (human subjects), IACUC… more
- University of Utah (Salt Lake City, UT)
- …review and approval of human research protections and compliance for the Institutional Review Board ( IRB ). Responsible for the comprehensive ... consistency, and compliance with regulations, guidelines, and institutional policies in preparation for IRB ...human research protections and IRB review processes for IRB employees, board… more
- Baptist Memorial (Memphis, TN)
- Overview Summary The IRB Coordinator III works under minimal or no supervision and acts as the lead staff for the IRB office. The IRB coordinator III ... is preparing IRB documents with accuracy. The IRB coordinator III prepares, extracts, manipulates, analyzes,...flow in the department. + Ensures department is maintaining compliance with research trial guidelines and sponsor… 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 ... compliance in one or more studies. Clinical Research Coordinator work includes study design, protocol...regulatory specialist in preparing for all local and Central 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 ... including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB...Board duties, budgeting duties, and assisting with patient research billing and reconciliation. + Ensures compliance … more
- University of Pennsylvania (Philadelphia, PA)
- …They may assist with Institutional Review Board ( IRB ) filings, sponsor and investigator filings and research related presentations. Participate in ... and resources, and much more. Posted Job Title Clinical Research Coordinator A/B (Cardiovascular Institute) Job Profile... Institutional Review Board ( IRB ) filings, sponsor and investigator filings and research… 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 ... including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB...Board duties, budgeting duties, and assisting with patient research billing and reconciliation. + Ensures compliance … 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 (Division of Urology/Department of...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 ... The Rabizadeh Lab team is seeking an outstanding clinical research coordinator to support their innovative ...including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB… more
- Johns Hopkins University (Baltimore, MD)
- …through recruiting and enrolling eligible patients into studies. + Prepare relevant documents for Institutional Review Board and as well for EPIC tracking. + ... Assist the PI in overseeing and maintaining institutional and federal regulatory compliance , including preparing the IRB initial application, annual 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 ... skills with an organization known nationally for excellence in research !** The Clinical Research Coordinator ...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 ... most advanced clinical trials in the world. The Clinical Research Coordinator I will work independently providing...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 ... with an organization known nationally for excellence in cancer research !** The Clinical Research Coordinator ...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 ... headache clinic within our Department of Neurology. The Clinical Research Coordinator I will work independently providing...including the Food and Drug Administration (FDA and local Institutional Review Board . **_*This position… 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 ... Board duties, budgeting duties, and assisting with patient research billing and reconciliation. + Ensures compliance ...and Drug Administration (FDA and local Institutional Review Board . + Maintains research … more
- Tufts Medicine (Lowell, MA)
- …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 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 ( Department of Medicine... submissions and renewals in accordance with FDA and IRB guidelines* Assure compliance with the protocol… 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 ... consent forms, and data use agreements. * Ensure compliance with institutional policies regarding data security, confidentiality, and research ethics. _Data… 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 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... submissions and renewals in accordance with FDA and IRB guidelines* Assure compliance with the protocol… more
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