- Dana-Farber Cancer Institute (Boston, MA)
- …Research Nursing, and other departments, as needed per the requirements of the clinical trial . + Responsible for organizing and preparing for both internal ... Research Program at Dana-Farber Cancer Institute is seeking a ** Clinical Research Coordinator (CRC)** to join our...for data entry of Subject Visit Tracking information into Clinical Trial Management System contemporaneously with medical… more
- Dana-Farber Cancer Institute (Boston, MA)
- …Research Nursing, and other departments, as needed per the requirements of the clinical trial . + Responsible for organizing and preparing for both internal ... life for all of those affected by cancer. The ** Clinical Research Coordinator (CRC)** will be an...for data entry of Subject Visit Tracking information into Clinical Trial Management System contemporaneously with medical… more
- Vanderbilt University Medical Center (Nashville, TN)
- …budgets, monitoring efficient invoicing and taking appropriate action to maintain clinical trial billing compliance, providing reports investigators, department ... and Alzheimer's Center seeks a qualified applicant for a Clinical & Translational Research Coordinator II position....prior to, during and after the conduct of a clinical /translational trial . Participates in periodic site visits… more
- Stanford University (Stanford, CA)
- Assistant Clinical Research Coordinator (1-Year Fixed-Term) **School of Medicine, Stanford, California, United States** Research Post Date Jun 17, 2025 ... is seeking a highly motivated and team-oriented full-time Assistant Clinical Research Coordinator . The work of the...Two Supportive Cancer Care Approaches is a 5-year funded trial by the PCORI to determine the best approach… more
- University of Pennsylvania (Philadelphia, PA)
- …be responsible for accurate data collection and overseeing the quality of the clinical trial data and records, scheduling and conducting study initiation and ... programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C - Epidemiology Division...System (CRMS) in real-time. This duty also includes maintaining clinical trial databases by completing case report… more
- University of Pennsylvania (Philadelphia, PA)
- …The research coordinator will be responsible for all aspects of clinical trial coordination including: subject recruitment, detailed data entry, subject ... Collect and report timely, valid, accurate data. Assist with the maintenance of clinical trial databases using REDCap functionality. Maintain subject files and… more
- University of Pennsylvania (Philadelphia, PA)
- …wealth of health and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C Job Profile Title Clinical Research ... Coordinator B Job Description Summary Clinical Research Coordinator B Responsible...subject data and patient tracking databases. + Assures reported trial data are accurate, complete and verifiable from source… more
- University of Utah (Salt Lake City, UT)
- …protocols ** Clinical Research Coordinator (Non-R.N.), II** Coordinate day-to-day clinical trial activities in adherence to Good Clinical Practices ... ** Clinical Research Coordinator (Non-R.N.), III** Coordinate day-to-day clinical trial activities in adherence to Good Clinical Practices (GCPs),… more
- University of Pennsylvania (Philadelphia, PA)
- …deviations and other unexpected events. + Coordinate independent central review of clinical trial end-points (eg, imaging data). Transport, process and ship ... programs and resources, and much more. Posted Job Title CLINICAL RESEARCH COORDINATOR B/C Job Profile Title...outcomes, and offer the best available innovative care to trial participants. The ACC CRU is instrumental in the… more
- Cedars-Sinai (Los Angeles, CA)
- …Degree Science, Sociology or related degree preferred. + Technical proficiency with clinical trial management systems and databases + Strong organizational and ... **Job Description** The Clinical Research Coordinator II works independently...screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed… more