- University of Miami (Miami, FL)
- …Department of SCCC has an exciting opportunity for a Full Time Clinical Research Coordinator 2 to work Hybrid at the UHealth Medical campus in Miami, ... FL. CORE JOB SUMMARY The Clinical Research Coordinator 2 (A) serves as a mid-level clinical research professional that assists in the planning, coordinating,… more
- Georgetown Univerisity (Washington, DC)
- …shared dedication to making a difference in the world. Requirements The Clinical Research Coordinator 2 (CRC2) is responsible for managing and coordinating 7 out ... week on site for these trials as the only coordinator for migraine/headache trials at our center, working exclusively...team of 6 CTM/CRC II s (including the CRC2), 2 Associate Directors, the Director of Clinical Trials, and… more
- Rush University Medical Center (Chicago, IL)
- …10. May assist PI with aspects of grant proposals. 11. May assist with Institutional Review Board assignments such as initial study approval, amendments, ... depending on the circumstances of each case. **Summary:** The Epi Research Coordinator 2 coordinates moderately complex Epidemiological, Behavioral or Human… more
- University of Miami (Miami, FL)
- …and participant compensation/reimbursement records. + Prepares and submits annual continuing reviews to the Institutional Review Board ( IRB ). + Notifies ... Palmer Eye Institute, has an exciting full time job opportunity for a Clinical Research Coordinator 2 in Miami, Florida. The Clinical Research Coordinator … more
- Stanford University (Stanford, CA)
- …regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to ... Clinical Research Coordinator 2 (Fixed-term 12 months) **School...applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are… more
- University of Miami (Miami, FL)
- …of Miami Health System, "UHealth" has an exciting opportunity for a Full-Time Clinical Research Coordinator 2 to work in the Peggy and Harold Katz Family Drug ... Discovery Center. The Clinical Research Coordinator 2 serves as a mid-level clinical...to approved protocols, help with study-related administrative tasks, facilitate across-the- board flow of information, and coordinate study activities and… more
- University of Miami (Miami, FL)
- …. This position is fully onsite in Miami, FL. The Clinical Research Coordinator 2 serves as a mid-level clinical research professional that assists ... monitoring, and evaluating of specific clinical research studies. The Clinical Research Coordinator 2 will work within the Division of Digestive Health… more
- Methodist Health System (Dallas, TX)
- …team members to provide the very best care for our patients. The Research Coordinator 2 perform coordination of all phases of the research process. The ... * Medical Assistant Certification, and/or a Certified Clinical Research Coordinator (CCRC) required * LVN or RN license, preferred...(CCRC) required * LVN or RN license, preferred * 2 or more years of related experience Your Job… more
- ICON Clinical Research (Mount Pleasant, SC)
- …information to an investigator in a timely manner, and immediately notifies investigators, the Institutional Review Board and sponsor of any serious adverse ... shape the future of clinical development. **Title:** Clinical Research Coordinator 2 (CRC 2 ) **Location:**...the trial for their trials as well as peer review of inclusion and exclusion for trials * Documents… more
- ICON Clinical Research (Cary, NC)
- …information to an investigator in a timely manner, and immediately notifies investigators, the Institutional Review Board and sponsor of any serious adverse ... you'll be helping shape an industry. **Title:** Clinical Research Coordinator 2 (CRC 2 ) **Location:**...the trial for their trials as well as peer review of inclusion and exclusion for trials * Documents… more
- University of Washington (Seattle, WA)
- …other members of the study team including but not limited to Research Study Coordinator 2 , graduate and undergraduate trainees. * Process human subject specimens ... to various institutional and external IRBs, ongoing tracking of annual IRB renewals, submission of annual reviews, modifications to existing protocols, SAEs, and… more
- Stanford University (Stanford, CA)
- …regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to ... Neurology at Stanford University is seeking a Clinical Research Coordinator 2 to conduct clinical research and...applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are… more
- University of Washington (Seattle, WA)
- …Generate initial drafts of human subjects' applications, consent forms and progress reports for institutional review board . * Serve as regulatory point of ... an excellent opportunity for a full time Research Study Coordinator 2 to work within our CVI...adherence. * Assist in the design of studies and review proposals to determine appropriate research methods. * Prepare… 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
- University of Colorado (Aurora, CO)
- …Office of Regulatory Compliance - Colorado Multiple Institutional Review Board ** **Job Title: IRB Panel Coordinator ** **Position #:00696471 - ... ** IRB Panel Coordinator ** **Description** **University of...the work flow to ensure that the Colorado Multiple Institutional Review Board (COMIRB) conducts… more
- University of Pennsylvania (Philadelphia, PA)
- …statistical software package and submit protocol modifications and continuing reviews to the IRB as needed, perform literature review , and write reports and ... will coordinate with the Project Manager to manage IRB protocols, project timelines, organize team meetings, including internal...and reporting out to the research team. Qualifications Research Coordinator : Bachelor Degree and 1 to 2 … more
- University of Pennsylvania (Philadelphia, PA)
- …protocols in accordance with Good Clinical Practices, HIPAA, and other federal/ institutional requirements, and ( 2 ) meet required obligations to ... Phase I, II, or III oncology clinical trials. + Assist the Regulatory Coordinator by preparing components of submissions (eg, institutional forms, initial… more
- University of Pennsylvania (Philadelphia, PA)
- …protocols; scheduling and conducting research visits; and submitting to both Penn and central Institutional Review Boards ( IRB ). This person will work in a ... Clinical Research Coordinator A Bachelor of Science and 1 to 2 years of experience or equivalent combination of education and experience is required.… 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** **Join our team!** 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