The Clinical Research Coordinator will work on multiple studies simultaneously. This position will work closely with the investigator(s) to develop protocols, case report forms, study budgets, manuals of procedure, standard operating procedures and recruitment materials. This position is responsible for all regulatory compliance for Penn studies for which this position is the lead coordinator. The research coordinator will prescreen and recruit participants for multiple complex protocols including both inpatient and outpatient studies. The research coordinator will properly consent and implement study visits including sample collection, data collection, entering orders into Epic, participant payment and management of the PennChart billing queue for all protocols for which this position is the lead coordinator.This position is responsible for regulatory management and compliance for a large national multicenter study with responsibilities including: ensuring that all regulatory documents are maintained within a custom data management system, IRB authorization agreements are developed for clinical sites operating under Penn’s IRB, and training coordinators at each site with regard to their regulatory responsibilities.
Penn has a long and proud tradition of intellectual rigor and pursuit of innovative knowledge, begun by Benjamin Franklin in 1740. That tradition lives today through the creativity, entrepreneurship, and engagement of our faculty, students, and staff. Academic life at Penn is unparalleled, with an undergraduate student body of 10,000 from every U.S. state and around the world. The entering class of 2015 is the most talented and diverse in Penn's history. Consistently ranked among the top 10 universities in the country, Penn welcomes an additional 10,000 students to our top-ranked graduate and professional schools.