Clinical Research Coordinator

Working 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 participants Obtaining informed consent from eligible participants Coordinating and conducting patient follow-up visits Maintaining accurate and complete source documentation Entering clinical data into electronic data capture (EDC) systems and responding to data queries Obtaining vital signs, ECGs, and other protocol-required assessments Performing basic laboratory procedures as permitted by the study protocol, including blood collection, centrifugation, specimen processing, storage, shipment, and reconciliation Coordinating medical record requests and maintaining appropriate documentation Maintaining study logs, regulatory files, and participant records Ordering, organizing, and tracking study-specific supplies Scheduling participant visits and conducting appointment reminders Developing and maintaining source documentation as required by individual protocols Supporting monitoring visits and addressing follow-up items in a timely manner Ensuring study reports, laboratory results, and other patient information are reviewed by the investigator as required Preparing and submitting safety reports, protocol deviations, and other required documentation to sponsors and/or the IRB Documenting and reporting adverse events in accordance with study requirements Escalating potential non-compliance or protocol issues to appropriate team members Maintaining professional and effective communication with study participants, internal teams, investigators, and external partners Following ALCOAC principles and applicable documentation standards Assisting with participant recruitment, enrollment, retention, and study tracking Maintaining confidentiality of participant, client, and organizational information Supporting study start-up activities, including completion of required training and maintenance of study documentation Assisting with preparation for and participation in site initiation visits and investigator meetings Setting up, maintaining, and supporting study-specific technology and systems as needed Performing other duties and responsibilities as assigned #J-18808-Ljbffr