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Clinical Trial Coordinator

  • 493694
  • Malvern
  • Palliative Care Research
  • Research
  • Maximum Term Part Time
  • Closing at: Jul 15 2022 at 23:55 AEST

Clinical Trial Coordinator - Malvern

  • Part Time – 2 full days per week contract
  • Work on Neurodegenerative and Aged Psychiatry trials
  • Immediate Vacancy – Apply Now!


About HammondCare

HammondCare are the leaders in aged and dementia care. We seek to improve the quality of life for people in need through palliative care, rehabilitation and mental health services for older people.

HammondCare is a leader in the research of neurodegenerative and aged psychiatry research and clinical trials.

Our Mission and Motivation is reflected in our passion to serve people with complex health or aged care needs, regardless of their circumstances.


More about the role

Reporting to the Clinical Trials Site Manager, the essence of this role is to work with the clinical trials team to ensure that all necessary activities are performed. You will learn and gain valuable experience and development in Cognitive Assessments and Data Analytics while working in a multi-disciplinary team.

Other duties include:

  • The administration and conduct of neurodegenerative and aged psychiatry trials.
  • Perform clinical trial start up activities (including ethics, governance and other trial specific activities).
  • Perform study specific procedures as required (e.g. venepuncture, cognitive rating scales, ECG’s, data entry & management).
  • Screen and identify potential patients with medical team support, ensuring all study-specific protocol criteria are met and appropriately documented.
  • Undertake the collection of data via questionnaires, tests, medical records and interviews.


About you (selection criteria)

We are looking for someone who has had strong experience in clinical trial research and an excellent understanding of Good Clinical Practice. Other requirements for the role include:

  • Qualification in nursing or a related field.
  • Excellent understanding of Regulatory and Ethics requirements (as demonstrated by relevant experience as a research assistant).
  • Excellent record keeping skills with a keen eye for detail.
  • Comfortable working within the spirit of site SOP’s
  • Ability to work independently and as part of a team (including demonstrated organisational and problem-solving skills).
  • Good communication and computer skills



  • 2 Days per week contract – out of Tuesday, Wednesday and Thursdays. Always have a long weekend!
  • Market comparative package including salary sacrificing benefits of working for a not-for-profit organisation.
  • Corporate Benefits – Reduced Healthcare memberships, Fitness Passport etc. Too many to list, but available on our website.

Ready to make a change? Apply Now!

Please ensure you CV is up to date and that your cover letter addresses the above selection criteria then hit “APPLY NOW”.



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