Clinical Research Associate

We are currently seeking a part-time, full-time or contract Clinical Research Associate.

You would be responsible for all aspects of clinical monitoring across a number of studies. This will include activities such as:

• Investigative site selection
• Drafting documentation for ethics and regulatory submissions
• Assisting with study initiation
• Overseeing and supporting patient recruitment
• Performing monitoring visits
• Overseeing investigational device accountability
• Evaluating study performance in view of patient safety and investigator compliance
• Data collection
• Close out visits

This role requires excellent interpersonal, written, verbal and organisational skills. Certification as a Clinical Research Associate is preferable. Applicants must have an ability to travel interstate and have a full Australian drivers license. In addition, a relevant tertiary qualification in Science or Nursing is essential, with recent experience within the last 5 years preferable. Experience working as a CRA in either a CRO or in industry is also required.

Our head office is based in Sydney and whilst we require the successful applicant to reside in Sydney or Melbourne, a flexible work arrangement is possible.

To apply for this position please email a copy of a current CV, with a brief description of how you consider yourself meeting the above selection criteria, to This email address is being protected from spambots. You need JavaScript enabled to view it.