We are seeking a detail-oriented Clinical Research Assistant to support the coordination and administration of clinical trials. This position will work closely with clinical research staff, healthcare professionals, and study participants to help ensure trials are conducted accurately, efficiently, and in accordance with established study protocols. Candidates must have a medical or clinical background and be comfortable working with medical terminology, patient information, and clinical documentation.

ResponsibilitiesAssist with the day-to-day coordination of clinical research studies and trialsSupport the screening and enrollment of potential study participantsReview medical records and study documentation for accuracy and completenessAssist with collecting and entering clinical trial dataMaintain organized and accurate study files and participant recordsCommunicate with patients regarding study visits, scheduling, and follow-upCoordinate appointments and study-related proceduresAssist research coordinators and clinical staff with study activitiesTrack study timelines, documentation, and outstanding requirementsHelp prepare documentation for monitoring visits and auditsFollow study protocols, HIPAA requirements, and applicable research proceduresCommunicate with physicians, research staff, sponsors, and other stakeholders as needed