Clinical Research Coordinator

6 days ago

Brisbane, Queensland, Australia Icon Group Full time
Clinical Research Coordinator - Research at Icon Group, Auchenflower

Research Brisbane Contract or Temp Research at Icon Group

Key Points
  • 12-month contracted; full-time position primarily based in Icon Cancer Centre Wesley.
  • Collaborate on Phase I - IV Clinical Trials in Oncology and Haematology
  • Training provided for candidates with relevant healthcare or research experience.
  • Join Australia's largest private cancer clinical trials program with access to cutting-edge technology and innovative care solutions.
The Opportunity
Be part of a dynamic and forward-thinking team dedicated to improving patient outcomes through innovative clinical trials. At Icon Group, we provide exceptional cancer care and deliver one of the most comprehensive private clinical trials programs in Australia.

Initially based at our Wesley location, this role is designed as a multi-site position, offering the flexibility to support other clinical trial centres within the group if needed. You will be joining a well-established, high-volume clinical trials unit, gaining exposure to Phase I to IV Clinical Trials in Oncology and Haematology.
About The Role
As a Clinical Research Coordinator, you will have access to leading technology and play a critical role in managing and conducting the clinical trial portfolio. This position is ideal for someone passionate about research and improving patient outcomes.
Key Responsibilities
  • Provide high level support to Icon Principal Investigators in the conduct and day to day management of clinical trials
  • Manage and conduct the clinical trial portfolio including the trial coordination, recruitment, participant and team member education and communication
  • Ensure that clinical research carried out within Icon is conducted in accordance with Good Clinical Practice, the NHMRC National Statement and Icon policies
  • Contribute to the financial management of the business unit to ensure that trial participants are tracked, and patient payment data is submitted in a timely fashion
  • Communicate effectively with trial participants to ensure that trial related procedures are booked appropriately and compliance to attendance for trial visits is maintained
  • Actively attend meetings with internal and external stakeholders
About You
You are a motivated, detail-oriented professional with excellent problem-solving skills and the ability to manage multiple priorities. Strong communication and interpersonal skills are essential for building relationships with stakeholders and ensuring trial success.
Essential Requirements
  • A background in medical oncology/haematology nursing, pharmacy OR
  • A bachelor's degree in health sciences, pharmacy, or a related allied health field, paired with relevant research coordination experience.
Desirable
  • Prior experience in Clinical Trials will be well regarded, but not essential as training will be provided.
  • Experience in Good Clinical Practice
To Apply
Please attach a resume and cover letter showing us why you'd love to join us, and what makes you a great fit for the role.Icon Group celebrates diversity and is committed to creating an inclusive workplace for all employees. We encourage applications from all diverse backgrounds.
Pre-Employment Vaccination Health Requirement
Icon is committed to managing the risk of transmission of specified vaccine preventable diseases (VPDs). Certain roles may require the successful candidate to show evidence that they have been vaccinated against or are not susceptible to specified VPDs.
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