Clinical Trials Manager – Oncology Trials

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Research
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Western Sydney Local Health District
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REQ690194 Requisition #
Employment Type: Temporary Full Time
Position Classification: Health Mgr Lvl 3
Remuneration: 137525 - 156231
Hours Per Week: 38
Requisition ID: REQ690194


Position Tagline
This is the 'enticer' for the candidate, this is the first few lines they will see when they see the ad on the sourcing site. Make sure it is appealing and compelling so the candidate is more likely to continuereading. e.g. Want to work in a world class medical facility? Be a part of a helping the community.

Where you'll be working
Organisation specific content
Short paragraph on the culture, benefits, what it's like to work here

What you'll be doing
In the last 15 years, the Westmead Medical Oncology Clinical Trial Unit (MOCTU) has undergone rapid expansion. Currently, the Unit employs a large team of highly qualified and experienced staff, including clinical trial coordinators, administrators, trial start-up officers, regulatory officers and financial administrators. The trial unit has around 90 active trials, ranging from phase 1 first-in-human to phase 4 trials with a high volume of recruitment.

This position will undertake a leading role for planning, running, expanding and improving the MOCTU service and managing the resources for the Unit, including personnel, finances and infrastructure.
  1. Relevant health related qualification and/or experience in the field of medical oncology clinical research and clinical trials.
  2. Extensive experience running clinical trials at site (public or private hospital).
  3. Demonstrated excellent leadership skills either as a line manager or as a mentor/trainer to Clinical Trial Coordinator role.
  4. Experience working in, or dealing with, sponsors and industry.
  5. Previous experience in clinical trial audits either Sponsor lead or regulatory body audits (for cause audits also acceptable).
  6. Demonstrated high level interpersonal, oral and written communication skills, such as negotiation and report writing applicable in both a research and administrative context.
  7. Demonstrated understanding of the legislation, codes and guidelines relevant to clinical and research ethics, and the NHMRC National Statement on Ethical Conduct in Human Research, relevant privacy acts and guidelines, the Human Tissue Act, and the Therapeutic Goods Act as it relates to use of medications in human research
  8. Proven highly developed delegation skills and staff coaching skills.


Need more information?
  1) Click here for the Position Description
  2) Find out more about applying for this position
For role related queries or questions contact Meenal Rai on meenal.rai@health.nsw.gov.au

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