- University of Washington (Seattle, WA)
- …The coordinator will oversee research billing compliance , maintain Institutional Review Board documents, modifications, and status reports. A key ... Care & Sleep has an outstanding opportunity for a Research Coordinator to join their team.** **POSITION...coordinator will be responsible for drafting and maintaining Institutional Review Board documents, modifications,… 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 ... before being reviewed by the IRB . Manages IRB documents, website, training compliance , files and...current knowledge of pertinent regulations for all types of research . Maintains a high level of time management skills… more
- HonorHealth (AZ)
- …Job 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...This includes initial determinations regarding expedited, exempt, or full board review , as well as human subject… more
- University of Colorado (Aurora, CO)
- …**Department: Office of Regulatory Compliance - Colorado Multiple Institutional Review Board ** **Job Title: IRB Panel Coordinator ** **Position ... Review Boards or OHRP/FDA regulations regarding human subject research + Certified IRB Manager (CIM) or...the work flow to ensure that the Colorado Multiple Institutional Review Board (COMIRB) conducts… more
- Covenant Health Inc. (Knoxville, TN)
- …conduct of clinical trials and human participant protection. In addition, the Clinical Research Nurse Coordinator assures compliance with protocol and ... Overview Registered Nurse Coordinator , Oncology Clinical Research Full Time,...storing all archived files. + Communicates effectively with patients, research team, IRB , sponsor, and Clinical Trials… 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
- 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 ... 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
- 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 ... 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
- 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 ... 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
- 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
- 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
- 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 ... 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
- 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 ... 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 Job Profile Title Clinical...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 ... generation of leaders in this exciting field. The Clinical Research Coordinator I will work independently providing...including the Food and Drug Administration (FDA and local Institutional Review Board . **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 ... 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
- 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)
- …duties and responsibilities as assigned Regulatory Responsibilities: + Prepare and process all Institutional Review Board ( IRB ) documentation through the ... and resources, and much more. Posted Job Title Clinical Research Coordinator B (Department of Gastroenterology) Job...physicians and coordinators' CVs and medical licenses, record of IRB certification and compliance ). + Resolve regulatory… 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