Location: Chicago, ILJob Description:Research Conduct/Study Management:Manages multiple concurrent moderately complex clinical trials that may include national level and multi-institutional pharmaceutical.Responsibilities include, but are not limited to, recruitment and screening of study subjects, obtaining informed consent, enrollment of subject in research study, subject follow-up, collecting and analyzing research data, completion of the case report form (CRF), adverse event reports and ensuring protocol adherence.Plans and coordinates subjects schedule for study procedures, return visits, and study treatment schedules; educates subjects about study procedures to be performed, what to report between and during visits,