Philadelphia, Philadelphia County
Jun 22, 2016

Duties: The Clinical Research Coordinator will manage the coordination of Phase I-IV multi-center clinical trials, involving technically advanced procedures with Radiology, including 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 close-out visits with Sponsor or CRO; adhere to all Penn ICF and FDA guidelines; prepare and process all IRB documentation.

Position is contingent on continued funding.

Qualifications: A Bachelor's Degree and 2 years to 3 years of experience or equivalent combination of education and experience is required. Effective problem solving capabilities, effective communication and writing skills are necessary, as well as the ability to multi-task and a demonstrated ability to work as part of a team or independently. Knowledge of IRB and human research protection regulations preferred. Experience with in-patient population is preferred.

Reference Number: 40-23186

Salary Grade: 026

Employment Type: Exempt

Org: DM-Gastroenterology

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

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