CLINICAL RESEARCH COORD B
Duties: The Clinical Research Coordinator B (CRC-B) will manage the coordination of Phase I-IV multi-center clinical trials, including coordination, organization and maintenance of all documentation required by Sponsor or CRO as well as working with partnering institutions on creating multi-center budgets, managing invoicing, and IRB paperwork under limited supervision and will need to use independent judgement; resolve data queries with Sponsor or CRO; recruit, screen and enroll potential study subjects; participate in the conduct of audits; process and ship blood and specimens; schedule patient visits and any necessary testing; obtain records required to complete case report forms; conduct initiation, monitoring and closeout visits with Sponsor or CRO; adhere to all Penn ICF, and FDA guidelines; prepare and process all IRB documentation. The CRC B will also manage clinical trials that involve hands-on technologically advanced and a special skill set involving investigational procedures with Radiology,
Qualifications: A Bachelor's Degree and 2 years to 4 years of experience or equivalent combination of education and experience is required. Effective problem solving capabilities, effective communication and writing skills are a necessity; as well as the ability to work independently or as part of a team. Knowledge of IRB and human research protection regulations preferred. Experience with in-patient populations is preferred.
Reference Number: 40-28862
Salary Grade: 026
Employment Type: Exempt
Job Family: I-Technical/Professional Research