Clinical Research Coordinator

Responsibilities

• Coordinate investigator-initiated and sponsored clinical research studies from start-up to close-out
• Manage study administration, including feasibility, ethics, governance approvals, and recruitment
• Maintain compliance with ICH-GCP, NHMRC, TGA, and organisational research governance requirements
• Oversee database management and data integrity, including REDCap setup and maintenance
• Manage project-related finances, including invoices, payments, and budget tracking
• Liaise with clinicians, investigators, sponsors, and CROs to support effective study delivery
• Support laboratory and specimen handling processes where applicable

Requirements

• Undergraduate degree in science, healthcare, or a related discipline
• Minimum 2 years of experience as a Clinical Research Coordinator or equivalent
• Sound knowledge of ethics, governance, and Good Clinical Practice (GCP)
• Proficiency with REDCap and clinical research databases
• Strong organisational, communication, and stakeholder engagement skills
• High attention to detail and ability to manage competing priorities

Benefits

• Salary packaging up to $15,900 pre-tax annually
• Access to one of Australia's largest educational scholarship programs
• Ability to purchase up to four additional weeks of leave
• Reduced cost of health services for you and your family at Epworth

About the Company

Epworth is Victoria’s largest not-for-profit private health care group, renowned for excellence in patient care, research, and innovation. We are an innovator in Australia’s health system, committed to fostering a diverse, inclusive, and culturally safe workplace where every patient matters.