Clinical Research Coordinator PT - Townsville

Job Description

Clinical Research Coordinator PT - Townsville Research QLD - Other Part Time Research at Icon Group Key Points Permanent part-time role, 4-day work week. Position based in Icon Cancer Centre Townsville, located at Hyde Park, QLD. Collaborate on Phase II - 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. This role is based at our site in Townsville, where you will be joining a well-established clinical trials unit, gaining exposure to Phase II to IV Clinical Trials in Oncology and Haematology. With plans to initiate new studies on-site, this is an exciting time to join our team and contribute to groundbreaking research that directly impacts patient care. 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 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. Work Requirements The part-time work arrangement will require you to work 60.8 hours a fortnight, or approximately 4-days a week. 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. #J-18808-Ljbffr