- Dayton Children's Hospital (Dayton, OH)
- …Department Specific Job Details: Required: Associates Degree 1-2 years of Research Assistant , Research Coordinator , or Regulatory Coordinator experience ... Children's - Main CampusDepartment:Surgery AdministrationSchedule:Part timeHours:20Job Details:The Clinical Research Coordinator will perform clinical research activities under the general… more
- Actalent (Tacoma, WA)
- …will have taken full responsibility in previous roles, not merely as a research assistant or backup coordinator . This role involves frequent use of EPIC and ... Oncology Clinical Research Coordinator Job Description We are seeking a dedicated...in cardiology and oncology. + Handle regulatory tasks, including IRB submissions. + Engage in sponsor correspondence, excluding budget… more
- 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
- Georgetown Univerisity (Washington, DC)
- …with an Associate's Degree and 5 years' minimum work experience as a Clinical Trial Coordinator or Clinical Research Assistant + In addition to a BA/BS or AA ... experience + 3 year minimum experience will be as a Clinical Trial Coordinator , Clinical Research Assistant , or equivalent position; However, as this is… more
- University of Utah (Salt Lake City, UT)
- …role will have significant responsibility for preparing, submitting, and maintaining institutional review board ( IRB ) protocols in coordination with ... 20. May perform functions required of the Clinical Research Assistant or Clinical Research Coordinator as necessary....experience in human subjects research, particularly institutional review board ( IRB )… more
- Cedars-Sinai (Los Angeles, CA)
- …staff meetings. + Works closely with investigators and regulatory staff or directly with Institutional Review Board ( IRB ) to submit adverse events, ... Diploma preferred. + 1 year of experience as a clinical research coordinator or clinical research associate/ assistant preferred. + Demonstrated ability to… more
- Stony Brook University (Stony Brook, NY)
- …The Program in Public Health at Stony Brook University (SBU PPH) seeks a staff assistant for the position of Program Coordinator for the Stony Brook Medicine ... Program Coordinator , Healthy Libraries Program **Required Qualifications (as evidenced...Writing:** * Assist HeLP leadership to prepare and submit IRB protocols to ensure use of de-identified human subject… more
- Catholic Health (Buffalo, NY)
- …may be credentialed as a Registered Professional Nurse (RN), Certified Research Coordinator (CRC), or Certified Medical Assistant + Candidates should also ... Schedule: Days Hours: 8:30am -4:30pm M-F Summary: The Research Coordinator is a healthcare position that will involve the...+ Knowledge of FDA rules and regulations, GCP, and IRB processes and procedures + Strong interpersonal and organizational… more
- University of Pennsylvania (Philadelphia, PA)
- …maintain all regulatory clinical trial documents and protocols ensuring compliance with the Institutional Review Board , the Abramson Cancer Center Trial ... Data Capture) or other programs. + Preparing study reports, annual reviews, and Institutional Review Board documentation + Liaising with key stakeholders,… more
- AdventHealth (Orlando, FL)
- …and adherence to research protocols._ _Serves as liaison between Principal Investigators and the Institutional Review Board ( IRB ) and the Office of ... **Clinical Research Coordinator II AdventHealth Orlando** **All the benefits and...research and administration._ _Reviews all elements of the current institutional IRB approved informed consent (IC) document,… more