Research Study Coordinator II, CCTRO New Trial Intake Coordinator) - Days - 40 Hours

General Summary Under minimal supervision, the Research Study Coordinator II, is responsible for: Coordinates research projects within guides of regulatory compliance and/or Code of Federal Regulation. Provides technical support to Principal Investigators. Duties Include But Not Limited To Interacting with both internal and external customers at all levels and oversight of recruitment and coordinating day-to-day operations of the study. Direct contact with potential and enrolled study participants expected. Provides other support as required. May work on multiple studies at any given time. Education/Experience Required Bachelor's degree in a scientific field, Psychology, Sociology, Anthropology, or related field. One (1) year of research project coordination experience. Certifications/Licensures Required SOCRA or ACRP and IATA certification preferred. Additional Information Organization: Henry Ford Medical Group Department: Cancer Clinical & Trans Resear Shift: Day Job Union Code: Not Applicable #J-18808-Ljbffr Henry Ford Health