Responsibilities:This role participates in the recruitment and screening activities to ensure successful enrolment of volunteers into studies scheduled at the Phase 1 Unit.Interfaces with research participants, to support efforts to determine eligibility and consenting of study participants according to protocol (R/S).The role interacts with the Principal Investigator and other study physicians, Recruiting/Screening department, Data Systems, and other personnel in support of study-specific activities.Top Skills:Fundamental working knowledge of clinical research.Able to review study protocols and educate study participants as part of the consent process.Ability to organize and prioritize responsibilities while paying close attention to detail.Able to work in a team-driven environment. 
