Clinical Research Coordinator- 256633

Key ResponsibilitiesWorking collaboratively with the clinical research site team, the CRC will support the execution of assigned clinical studies. Responsibilities may include:Screening and pre-qualifying potential study participantsObtaining informed consent from eligible participantsCoordinating and conducting patient follow-up visitsMaintaining accurate and complete source documentationEntering clinical data into electronic data capture (EDC) systems and responding to data queriesObtaining vital signs, ECGs, and other protocol-required assessmentsPerforming basic laboratory procedures as permitted by the study protocol, including blood collection, centrifugation, specimen processing, storage, shipment, and reconciliationCoordinating medical record requests and maintaining appropriate documentationMaintaining study logs, regulatory files, and participant recordsOrdering, organizing, and tracking study-specific suppliesScheduling participant visits and conducting appointment remindersDeveloping and maintaining source documentation as required by individual protocolsSupporting monitoring visits and addressing follow-up items in a timely mannerEnsuring study reports, laboratory results, and other patient information are reviewed by the investigator as requiredPreparing and submitting safety reports, protocol deviations, and other required documentation to sponsors and/or the IRBDocumenting and reporting adverse events in accordance with study requirementsEscalating potential non-compliance or protocol issues to appropriate team membersMaintaining professional and effective communication with study participants, internal teams, investigators, and external partnersFollowing ALCOAC principles and applicable documentation standardsAssisting with participant recruitment, enrollment, retention, and study trackingMaintaining confidentiality of participant, client, and organizational informationSupporting study start-up activities, including completion of required training and maintenance of study documentationAssisting with preparation for and participation in site initiation visits and investigator meetingsSetting up, maintaining, and supporting study-specific technology and systems as neededPerforming other duties and responsibilities as assigned