Regulatory Assistant

Description: Will assist other regulatory coordinators with their duties. This position will focus primarily on pharmaceutical sponsor studies. This is a group of individuals who handle all of administrative work for the active and continuing studies regulatory work. They will work with PIs, clinical coordinators and the IRB to make sure regulatory documents are approved and correct for all of the pharmaceutical research studies in medical oncology. The regulatory coordinators and assistants do not work with patients or in the clinics at all.