CLINICAL RESEARCH COORD C
Duties: Independently manage Phase I-V clinical trials, Recruit, consent and screen patients according to protocol. Schedule patient visits and any necessary testing, Monitor patients per protocol requirements and ensure adherence to protocol requirements, Organize and maintain all documentation required by the sponsor or CRO - includes source documentation, case report forms, and research charts. Collect, review and report study data, complete case report forms and resolve data queries, process and ship study specimens including blood, urine and tissue samples. Participate in initiation, monitoring, audit and close-out visits, Participate in study team meetings, disease site group meetings, and ongoing protocol training/compliance meetings, Assist in the development/maintenance of study specific case report forms and source document tools. Assist in the training of new clinical research coordinators. Show vigilance in patient safety, protocol compliance and data quality. Adhere to all University of Pennsylvania, FDA and GCP guidelines.
Position is contingent on continued funding,
Qualifications: Bachelor's degree and 4-6 years of experience or an equivalent combination of education and experience is required.
Effective problem solving abilities; effective communication and writing skills; strong organizational and time management skills; flexible and able to multi-task; demonstrated ability to work as part of a team, as well as independently; knowledge of IRB and human research protection regulations.
Reference Number: 40-24839
Salary Grade: 027
Employment Type: Exempt
Org: CC-Cancer Center
Special Requirements: Background check required after a conditional job offer is made. Consideration of the background check will be tailored to the requirements of the job.
Job Family: I-Technical/Professional Research