Ballarat Oncology and Haematology Services – Ballarat VIC Clinical / Medical Research (Healthcare & Medical) About us: Ballarat Oncology and Haematology Services is a successful private practice in Ballarat.
We are a passionate team of health care professionals and support staff, united by a common goal to deliver the best possible life outcomes for our patients.
Our dedicated team takes pride in providing positive and respectful patient care in the fields of haematology and oncology.
About the role: You will be a key member of our Team.
The Clinical Research Nurse Coordinator (CRNC) will support current and upcoming Clinical Trials by working with colleagues and members of multidisciplinary teams to ensure a high quality of data collection and successful Trial management.
The CRNC will be responsible for the coordination and management of a dedicated portfolio of Clinical Trials, involving liaison, patient education, and coordination, to ensure the highest standard of care is delivered to all Clinical Trial patients.
This role will be based within the Clinical Trials Unit of Ballarat Oncology and Haematology Services.
It is offered as a permanent part-time position comprising a nine-day fortnight.
You will provide operational support for the day-to-day execution of Clinical Trials, and you will ensure study specific information is communicated effectively and professionally to all parties involved.
Job description: Clinical Research Nurse Coordinator (Health Professionals and Support Services Award) This is a permanent part-time position involving setting up and coordinating concurrent Clinical Trials within this busy unit.
The position is a 9-day fortnight, and the role is based in Ballarat Victoria.
This role will suit a nurse who is keen to learn more about research methodology and regulatory processes that govern drug development in Australia, while working closely with Clinical Trial participants and their families.
The Clinical Research Nurse Coordinator will have responsibility for the delivery of direct and indirect care and associated data collection for concurrent research studies undertaken in the unit.
The Clinical Research Nurse Coordinator will work in partnership with members of the multidisciplinary teams to ensure that the highest standard of care is delivered to all patients involved in Clinical Trials and, where relevant, their families.
The Clinical Research Nurse Coordinator will maintain an excellent standard of clinical care and research integrity, in compliance with the National Health and Medical Research Council (NHMRC) National Statement on Ethical Conduct in Human Research 2023 and the internationally accepted ICH Guideline for Good Clinical Practice (GCP).
The Clinical Research Nurse Coordinator will work in close partnership with the Clinical Trials Assistant.
This will include ensuring timely and accurate data entry, collection, processing, and shipment of laboratory samples at each protocol-mandated timepoint.
Key staff interactions include liaising with Oncologists, Administration and Reception staff, Oncology Nursing Staff, and staff from support services such as Trial Pharmacists, Radiology, Pathology, Health Information Services, Clinical Trial Associates, Trial Sponsors, and the Ethics Committee.
How to apply: We welcome applications from suitable candidates.
Please email ****** to request the key selection criteria for this position.
Should you fulfil the key selection criteria and then wish to apply, please provide your cover letter which should specifically address your skills and experience, and a copy of your resume with two professional referees.
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