Duties: The primary function of this position is to coordinate imaging trials within the Neuroradiology Clinical Research Division in the Department of Radiology. Responsibilities will include screening, recruiting, and consenting patients; managing trials with investigational imaging contrast agents; organizing and maintaining study documentation; performing data entry; resolving data queries; reviewing medical records; scheduling study-related procedures and tests in EPIC/Pennchart, Radiology, and other research systems; preparing and processing of regulatory documentation to IRB and other regulatory committees; interaction with the study sponsors, preparation and participation in study initiation visits, audits, monitoring and closeout visits. Perform additional duties as assigned.

Position is contingent on continued funding.

Qualifications: Bachelor's Degree and 2-4 years experience or equivalent combination of education and experience required. Effective oral, written, organizational and interpersonal skills. Ability to manage several projects simultaneously, work independently, and work as part of a team. Good communication skills and experience with direct patient contact. Experience in a research work setting with attention to detail and accuracy in data collection and management; knowledge of IRB, human subject protection regulations, and good clinical practice. Experience with Radiology imaging modalities preferred. ACRP and/or SoCRA clinical research certification desired.

Reference Number: 40-25110

Salary Grade: 026

Employment Type: Exempt

Org: RA-Radiology

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

Similar jobs

Similar jobs