Clinical Research Coordinator – Blacktown (Part-Time, 16 hours/week) Start Date: immediately Duration: Approximately 6 months Working Days: Wednesday and Friday Key Responsibilities Maintaining and updating study documentation, including protocols, case report forms (CRFs), and Electronic Data Capture (EDC) systems Supporting patient screening and enrollment, including handling informed consent and privacy documentation Coordinating logistical activities for study procedures in line with the study protocol Performing data entry, quality checks, and resolving queries to ensure data accuracy and completeness Managing and shipping biological samples Communicating with study monitors and responding to study-related inquiries Help with patient recruitment, patient education and community outreach Carrying out general administrative tasks related to the study Your Profile Bachelor’s degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting (e.g., clinical research coordinator, research assistant, nurse, medical assistant) Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedules Good knowledge of medical terminology Strong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access) Must have at least 1-2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site Excellent interpersonal and communication skills Strong organizational skills and attention to detail #J-18808-Ljbffr