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Clinical Research Coordinator - Oncology

NSW Government - Sydney, NSW

Health, Medical & Pharmaceutical
Source: uWorkin


Employment Type: Temporary Full Time until 03 July 2022
Position Classification: Scientific Officer
Remuneration: $64,474.97 - $93,390.77 per annum
Hours Per Week: 38
Requisition ID: REQ237096

Position Tagline

The Oncology Clinical Research Unit, Cancer Care Centre, St George Hospital, is seeking an enthusiastic clinical research coordinator to work in cancer clinical trials. This exciting opportunity will enable you to start your career in clinical research or further develop existing skills in a leading clinical research centre dedicated to improving the lives of people with cancer through research and quality care. The role is a 12 month temporary full time position with the possibility of renewal subject to funding and work.

Where you'll be working
Oncology Clinical Research Unit, Cancer Care Centre, St George Hospital

What you'll be doing The vision for South Eastern Sydney Local Health District (SESLHD) is ‘exceptional care, healthier lives’. SESLHD is committed to enabling our community to be healthy and well, and to providing the best possible compassionate care when people need it.

The Clinical Research Coordinator manages all aspects of oncology research from feasibility and planning through to implementation, participant enrolment and management, study conduct, regulatory compliance, data management, study close-out and archiving. The role is fundamental to delivering, managing and upholding the quality standards of the research conducted.

SESLHD is committed to creating a workplace that reflects the diversity of our community. This will help ensure our employees, our patients and their carers, feel supported. We encourage people from different backgrounds to apply.

Employment of a temporary visa holder may only occur if no suitable permanent resident or citizen of Australia has been identified for this position following suitable labour market testing.

  1. Bachelor Science degree.
  2. Experience in clinical trial coordination and procedures or proven knowledge of the clinical trial and research regulatory environment and processes as per ICH-GCP standards.
  3. Attention to detail and ability to deliver accurate and complete documentation.
  4. Demonstrated ability to function effectively as a member of a team.
  5. Excellent time management skills, ability to prioritise, manage competing tasks and meet deadlines.
  6. Excellent computer skills, particularly Microsoft Office (outlook, word, excel, powerpoint, access).
  7. Demonstrated critical thinking, problem solving and organisational skills.
  8. Highly developed verbal and written communication skills.

Need more information?
1) Click here for the Position Description and SESLHD Expected Standards
2) Find out more about applying for this position
For role related queries or questions contact Peter Fink on [email protected]

Applications Close: 04 July 2021

Sydney, NSW

Health, Medical & Pharmaceutical


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