Clinical Trials Coordinator - Radiation Oncology
Ingham Institute for Applied Medical Research (‘Ingham Institute’) is an innovative and growing not-for-profit organisation, committed to our vision of Inspiring Health and Transforming Care. At Ingham Institute we make and apply discoveries that translate into radical improvements in health, and healthcare for all.
We work closely with the Southwestern Sydney Local Health District, Western Sydney University, University of New South Wales, and have ambitious growth plans that will see us expand to be a multi-centre Institute (Liverpool, Macarthur, and Bankstown).
About the role
The Radiation Oncology Clinical Trials Unit is currently recruiting for a Clinical Trial Coordinator to join the growing group based in Ingham Institute at Liverpool.
The Radiation Oncology Clinical Trials Coordinator will be responsible for a range of duties that support the cancer trials and research portfolio. The position will support the Radiation Oncology clinical trials unit with all trial activities of the unit and will hold responsibility for research data management support and study coordination as directed.
We currently have a 12-month contract available and can be flexible between Part-Time (from 0.6 FTE) or Full-Time (1 FTE) hours.
As an experienced coordinator, you will undertake some of the following:
* Effective management of research and clinical trials processes.
* Effective management of patient bookings/appointments for medical and nursing staff in regard to clinical trials, ensuring a professional and efficient client service delivery.
* Comply with GCP requirements.
* Supportive relationship with other radiation oncology departments and other clinical trials groups.
* Timely submission of data.
* Maintenance of patient folders.
* Effective maintenance of screening and accrual and reports record keeping.
* Supportive relation with HREC office.
The ideal candidate will meet the following essential criteria:
* Tertiary qualification at a graduate level in a health or science discipline.
* A minimum of 1-year previous experience in sponsored clinical trials.
* Proven working knowledge of the clinical trial and research regulatory environment and processes as per ICH–GCP standards.
* Experience in clinical trial coordination or research project management.
* Strong communication skills (verbal, written and virtual).
* A high level of professionalism.
* Positive, “can do” attitude.
* Strong problem-solving skills, which are solutions focused.
* Ability to work independently and as part of a multidisciplinary clinical team.
* Strong attention to detail and highly organised.
* Demonstrates proficiency in a range of computing skills including word processing, databases, and spreadsheets and their application in research.
* Excellent time management skills, ability to prioritise and manage competing tasks and meet deadlines.
To be a suitable candidate, your application must include a cover letter addressing the listed essential criteria demonstrating suitability to the role from your previous experience.
The successful candidate will be required to undergo a National Police Check.
Applications will only be considered from those candidates eligible to work in Australia.
Please note that only short-listed applicants will be contacted.
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