CLINICAL RESEARCH COORD A/B
Duties: The Clinical Research Coordinator A will assist in the coordination of Phase I-IV clinical trials, including coordination, organization and maintenance of all documentation required by Sponsor or CRO; resolve data queries with Sponsor of 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 close-out visits with Sponsor or CRO; adhere to all Penn ICF and FDA guidelines; prepare and process all IRB documentation.
The Clinical Research Coordinator B, in addition to above, will manage multi center clinical trials, including working with partnering institutions on budgets and IRB paperwork. The CRC B will have limited supervision in the management of clinical trials and will need to use more independent judgement.
Qualifications: Bachelor's degree and 1 year to 3 years of experience or equivalent combination of education and experience required for the A position; 2 years to 4 years of experience or equivalent combination of education and experience required for the B position. Effective communication and writing skills, as well as the ability to multitask are necessary for this position. Must be able to work independently or as part of a team. Knowledge of IRB and human research protection regulations preferred.
Reference Number: 40-28363
Salary Grade: 025/026
Employment Type: Exempt
Job Family: I-Technical/Professional Research