About the role
Position Summary
Coordinates and administers research study associated activities under the direction of the Principal Investigator (PI) and Research Nurse Manager/Supervisor. Assists in project planning; coordinates and implements clinical research; acts as the patient advocate by assuring the safety, consistency, and accuracy of the treatment regimen as dictated by the PI and the protocol, and coordinates all activities specifically related to the implementation of the treatment regimen, including consenting subjects when appropriate, scheduling appointments and ancillary services, registering patients for billing compliance and data collection. Remains current in all regulatory education, training and certification requirements.
Education
Bachelor`s degree or minimum ten years experience as a study coordinator required. Preferred, CPR Phlebotomy, IATA and CCRP or CCRC certification upon hire or to be obtained as appropriate. Maintains CITI certification and ongoing knowledge of ICH-GCP, fe
Experience