Avance Clinical is a full-service CRO with an international reputation for delivering high quality clinical trial results. We facilitate quality drug development by aligning our people, their skills and expertise in the pursuit of a healthier world. 

Avance Clinical recognises that our most important asset is our people. We offer a work environment and a culture that values honesty and respects its people.

We value the different skills, backgrounds, experiences and perspectives of our people and we focus on the skills and expertise that each of them bring to the organisation. We’ll provide you with opportunities to build your skills and progress your career. We are committed to providing a challenging and stimulating environment where what our people do matters.

As our organisation continues to grow, we want our people to grow with it. We invest in training and development programs, give our people opportunities to learn and, and when they are ready encourage them to accept greater challenges and responsibility along the way.

At our heart is a belief in the potential in each other and our clients, it unites and motivates us. We believe that our values and behaviours lay the foundations of our culture.

At Avance Clinical you will enjoy:

  • a challenging and stimulating environment where what you do matters
  • a diverse and inclusive culture with a strong emphasis on team collaboration
  • training and career development opportunities
  • attractive remuneration 

Current Positions Available

Please see below for positions currently available at Avance.  Alternatively, should there be no current vacancies listed then please forward your CV and cover letter to careers@avancecro.com for consideration for future opportunities.


Avance Clinical is now on a new phase of growth with new shareholders who are looking to invest for the future.

An opportunity exists for an experienced SCRA or CRA to join the team at Avance. This is a full-time permanent position with an immediate start for the right applicant. Interstate travel is a requirement of this role.

Acting as the primary link between sites and sponsor, you'll be responsible for:

  • Performing start-up, initiation, monitoring and close-out visits along with maintaining appropriate documentation
  • Developing your skills and knowledge on clinical trials within a wide scope of therapeutic areas
  • Monitoring all aspects of studies to ensure compliance with GCP, study protocol and regulatory requirements and prepare monitoring reports
  • Development and review study protocols and other study related documents
  • Preparing ethics submissions and assist in preparation of Clinical Study Reports.

To be successful in this role you will need to have prior experience monitoring clinical trials, ideally within Australia and/or New Zealand. 

It is essential that you have a degree in science or other healthcare related discipline, at least 3 - 5 years experience working as a SCRA/CRA and 3-5 years experience in the pharmaceutical industry / CRO. You will have sounds knowledge of Australian and New Zealand drug development process, clinical trial monitoring procedures, GCP guidelines and medical terminology.

For further information about this interesting opportunity with Avance Clinical and to apply, please click here.

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