- University of Pennsylvania (Philadelphia, PA)
- …in patient safety, protocol compliance and data quality. + Communicate clinical trial patient activity to the investigational drug pharmacy (IDS) to ... programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C Job Profile Title...performed. He/she will be responsible for all aspects of clinical trial coordination including subject recruitment, detailed… more
- University of Pennsylvania (Philadelphia, PA)
- …in patient safety, protocol compliance and data quality. + Communicate clinical trial patient activity to the investigational drug pharmacy (IDS) to ... programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C Job Profile Title...accurate data collection and overseeing the quality of the clinical trial data and records, scheduling and… 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)
- …for making sure study timelines and goals are met. Independently move a clinical trial through each phase of development, resolving issues and queries ... of health and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C (Department of Medicine) Job Profile Title … more
- University of Pennsylvania (Philadelphia, PA)
- …conduct of clinical research studies, including the recruitment and retention of clinical trial participants. Schedules and runs study visits as per ... programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C Job Profile Title... research studies, including the recruitment and retention of clinical trial participants. Schedules and runs study… more
- University of Pennsylvania (Philadelphia, PA)
- …for making sure study timelines and goals are met. Independently move a clinical trial through each phase of development, resolving issues and queries ... health and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C (Division of Infectious Diseases) Job Profile Title… more
- University of Pennsylvania (Philadelphia, PA)
- … research performed. He/she will be responsible for all aspects of clinical trial coordination including subject recruitment, detailed data entry, subject ... programs and resources, and much more. Posted Job Title Clinical Research Coordinator B (Department of Gastroenterology)...screen and enroll potential study patients as specified per protocol . + Participate in the conduct of audits by… 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, ... programs and resources, and much more. Posted Job Title Clinical Research Coordinator C (Department of Neurosurgery)...trials + Recruit, consent and screen patients according to protocol + Schedule patient visits and any necessary testing.… more
- University of Pennsylvania (Philadelphia, PA)
- …and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator A (Department of Endocrinology, Diabetes and Metabolism) ... Job Profile Title Clinical Research Coordinator A Job Description Summary...tasks involved in remote and site study visits per protocol . Assist with performing clinical assessments as… more