- University of Utah (Salt Lake City, UT)
- …obtaining current treatment roadmap for all inpatients. 7. Download information from clinical trial websites and maintain communication with consortiums as ... Details **Open Date** 05/02/2025 **Requisition Number** PRN41797B **Job Title** PS Clinical Research Coord **Working Title** PS Clinical Research Coord **Job… more
- Touro University (Hawthorne, NY)
- Overview Responsible for pre- clinical trial set up, initial and ongoing regulatory submission and IRB activities, subject screening and enrollment, specimen ... compliance with the Good Clinical Practice guidelines in clinical research. + Monitor study patients for adverse events in collaboration with clinical… more
- University of Pennsylvania (Philadelphia, PA)
- …of the study team. They will be responsible for all aspects of clinical trial coordination including subject recruitment, detailed data entry, subject visits, ... and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator C (Department of Neurosurgery) Job Profile Title Clinical… more
- Mount Sinai Health System (New York, NY)
- …testing + Secure, deliver, and ship blood and/or tissue samples, radiographs, and other clinical trial specimens as required by protocol + Act as liaison between ... **Job Description** A Clinical Research Coordinator II position is currently available...Attend divisional/departmental/institutional education and training seminars + Facilitate sponsor monitor visits + Educate new staff regarding overview of… more
- Community Health Network (Indianapolis, IN)
- …investigators in identifying, screening, interviewing, and consenting eligible patients for the clinical trial and completing the associated data entry and ... Clinical Research Specialist Job Ref 2502284 Category Administrative...regulations as needed and as trained + Participates in monitor and regulatory audits and routine department meetings as… more
- Defense Health Agency (Fort Sill, OK)
- …materials required for the performance of test procedures. Implement and monitor quality control procedures. Recognize, locate, and implement corrective action to ... information about transcripts is in this document. Basic Requirement for Clinical Laboratory Scientist: A. A Bachelor's or graduate/higher level degree from… more
- UTMB Health (Galveston, TX)
- … Research Monitor or Coordinator experience + Experience with a Clinical Trial Management System (CTMS), electronic IRB platform and EMR **LICENSES, ... Clinical Research Coach (Research Administration - Galveston) Certified...or CCRP **Galveston, Texas, United States** Research Academic & Clinical UTMB Health Requisition # 2405989 **Minimum Qualifications:** Bachelor's… more
- Defense Health Agency (Fort Riley, KS)
- …new specimen if determined to be unusable. Select, perform, evaluate, and monitor the performance of test procedures using manual and/or automated techniques in ... information about transcripts is in this document. Basic Requirement for Clinical Laboratory Scientist: A. A Bachelor's or graduate/higher level degree from… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …preference. KEY RESPONSIBILITIES: + Independently manages significant and key aspects of a large clinical trial or all aspects of one or more small trials, or ... up-to-date and complete throughout the course of the research projects. 5. Clinical Monitoring: Monitor participants' progress throughout the trials, and… more
- HCA Healthcare (St. Louis, MO)
- …Do you want to join an organization that invests in you as a ** Clinical Resources Manager** ? At HealthTrust Performance Group, you come first. HCA Healthcare has ... make a difference. We are looking for a dedicated Clinical Resources Manager like you to be a part...coordination with key stakeholders for site selection, development of trial /pilot feedback forms, collection of forms, analysis of responses,… more