Lead Clinical Research Program Coordinator bei University of Pittsburgh

Coordinates high-level, protocol-related research procedures and study components and manages one study or assists with larger studies. Ensures the safety of the research and laboratory. Manages staff, audits studies, and recommends policy improvements.

Coordinates high-level, protocol-related clinical research procedures and study components and manages one study or assists with larger studies. Leads development of study protocols individually or with team input. Ensures the safety and quality of the research and laboratory samples and data. Participates in or leads (as needed) clinical research enrollments. Audits studies, and recommends policy improvements. Phlebotomy certification and the ability to drive a vehicle for access to research sites are required.  
 

Mostly sedentary. May be required to lift up to 25 lbs.