Duties: Assist in the coordination of Phase I-IV clinical trials in the field of cardiac electrophysiology, including, preparation of regulatory documents and IRB correspondence; 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 Investigator, 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 and urine; Participate in initiation, monitoring, audit and close-out visits; Participate in study team meetings, and ongoing protocol
training; Show vigilance in patient safety, protocol compliance and data quality; Adhere to all University of Pennsylvania, FDA and GCP guidelines

Qualifications: A Bachelor's degree and 1 year to 3 years of experience or an equivalent combination of education and experience required.

Reference Number: 40-30789

Salary Grade: 025

Employment Type: Exempt

Org: DM-Cardiovascular Medicine

Special Requirements:

Job Family: I-Technical/Professional Research