Pre-Screening ScreeningRecruitingEnrollment of study participants into clinical trials. Consenting conducting study appointments and procedures. Gathering study data and data entry.Coordination of study visits and study procedures. Maintaining regulatory and study documentation. Creating source documents keep appropriate logs track participants throughout their participation. Maintaining study specific training.Collecting study specimens processing and shipping. Maintaining study supply and equipment inventory.Communication between study team and sponsors and vendors. Attending team meetings with Principal Investigator. Update Principal Investigator and supervisor on study status. Prepare and attend monitor and audit visits.Work closely with Principal Investigators to coordinate and execute all aspects of multiple clinical trials. Work with CRC I team members to mentor share knowledge and help train.Trained in phlebotomy and biospecimen collection.Knowledge Skills & AbilitiesMust possess excellent interpersonal skills.Knowledge of working in a clinical setting.Ability to work independently and in a team.Ability to maneuver multiple tasks at once.Knowledge of Cerner OnCore ReCap.