Working closely with Principal Investigators, associated research staff and site staff, you will co-ordinate and support clinical trial research activities conducted at the Hospital.
This role will require you to ensure that a high quality, professional and efficient research service is provided consistently and in accordance with Good Clinical Practice and appropriate clinical trial regulations.
You will be reporting to the Clinical Trials Manager and the role will involve, but is not limited to;
Provide preliminary explanation of clinical trials and clinical research projects to patients and families as required.
Facilitating a high standard of clinical trials care by liaising with the medical and nursing staff delivering the care to the patient, and interacting with patients and their caregivers / family members regarding the patient's participation in research;
Liaise with local pathologists to collect pathology specimens as required.
Ensure up-to-date source records are available for clinicians and assist in all aspects of protocol procedures.
Data management
Co-ordinate trial medication supply where appropriate.
Assessing patient eligibility for clinical trials and performing randomisations where appropriate.
About You
To succeed in this role, you will demonstrate the ability to lead and work in a multidisciplinary health care team environment with a commitment to high professional standards in all aspects of work.
Your excellent communication and organisation skills, attention to detail, understanding of the importance of confidentiality and data integrity is critical for this role.
The successful candidate will also meet the following criteria:
Registered or Enrolled Nurse currently authorised to practice by AHPRA or equivalent allied health or science qualification




Demonstrated understanding of clinical trials methodology and knowledge of Good Clinical Practice (ICH-GCP) requirements
Ability to develop rapport with patients and their families in stressful situations
Computer software, informatics, data collection and/or media skills
Candidates that meet the following criteria will be highly regarded:
Substantial working experience in a research or clinical environment, including experience in the conduct and coordination of clinical trials
Experience in the area of oncology and/or Haematology
Understanding of ethics and governance in clinical research
What's in it for You:
At Ramsay, we care for our people by offering benefits that truly support your career, wellbeing and lifestyle, including:
Grow your careerwith recognition programs, employee referral bonuses, scholarships, free access to LinkedIn Learning and the Ramsay Leadership Academy
Save more every daywith Ramsay Rewards, giving you exclusive deals at 100+ retailers, restaurants, travel providers and more
Enjoy peace of mindwith lower hospital cover costs and higher extras limits on services like General and Major Dental, plus pharmacy and allied health discounts
Find balancethrough adaptable rostering options, flexible leave and access to free, confidential counselling and wellbeing support 24/7
Increase your take-home paythrough salary packaging and novated leasing, plus discounts on leisure travel, gyms and lifestyle services.
Why Join Ramsay:
At Ramsay Health Care, "people caring for people" is at the heart of everything we do.
We are:
Australia's largest private hospital operator, with over 74 sites and 35,000 staff
A values-led workplace where you'll be supported personally and professionally
A place with flexible, permanent and career-growth opportunities nationwide.

📌 Clinical Trial Coordinator (Gold Coast)
🏢 Recognized
📍 Gold Coast