Clinical Trial Coordinator

Clinical Trial Coordinator HomeNurse4U Wellington, New Zealand We are seeking an organized and compassionate Clinical Trial Coordinator to join our on-site research team. In this role, you will champion patient safety and data integrity while executing clinical trial protocols from screening to study closure. You will work closely with the Principal Investigator (PI) to manage patient visits, collect critical study data, and ensure seamless daily operations. Key Responsibilities - Duration : 3-4 Months Pre-screen potential participants by reviewing medical charts and histories to assess preliminary eligibility against protocol-specific inclusion/exclusion criteria. Coordinate and conduct the informed consent process, ensuring patients fully understand the study's requirements, risks, and benefits. Schedule and manage screening visits, working with the PI to confirm final eligibility before enrollment. Patient Visits & Clinical Operations Manage day-to-day scheduling, confirming patient appointments and coordinating any required transportation. Perform clinical duties and preliminary assessments as permitted by certification and protocol guidelines (e.g., measuring vital signs, collecting medical history, performing ECGs, or drawing blood). Administer patient questionnaires, dispense investigational products (IP), and track study medication compliance. Act as a patient advocate, addressing participant inquiries and relaying feedback or reported symptoms to the PI or study doctor. Data Management & Compliance Accurately document study visits, source documents, and Case Report Forms (CRFs) in accordance with Good Clinical Practice (GCP) and ALCOAC principles. Report and log any adverse events (AEs) promptly, escalating critical issues to the PI and sponsor. Clinical Trial Coordinator Wellington, New Zealand #J-18808-Ljbffr