Senior/ Clinical Research Associate - Site Management (Adelaide or Perth)

Quintiles Australia are currently looking for an experienced Senior Clinical Research Associate (SCRA) or Clinical Research Associate (CRA) (depending on your level of experience) to be part of our highly successful Site Management/ Clinical Operations team. This position is full-time and ongoing, however suitably experienced part-time SCRAs may also be considered at 4 days/wk. The successful candidate will be home based out of Adelaide OR Perth. Please note – as this position is for a home based CRA we require someone with at least 18 months prior CRA/ monitoring experience, this role is not suitable for entry level candidates.

As you develop your career as a CRA, this role offers you the opportunity to plan and progress your career in the direction you choose. At Quintiles, we do not believe in a ‘career ceiling.’ You can make the Senior/CRA role a stepping-stone into wider opportunities like operations management, dedicated customer solutions, and project management. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards.

Award winning and innovative, we will give you access to cutting-edge in-house technology, allowing you to work on global projects but with a regional / home state travel remit, so no need for national travel in certain countries. You will be building a smart and flexible career with no limits.

While projects vary, your typical responsibilities might include:

  • Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
  • Supporting the development of a subject recruitment plan
  • Establishing regular lines of communication plus administering protocol and related study training to assigned sites
  • Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
  • Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution

You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.

You should have:

  • A Bachelor’s degree in a health care or other scientific discipline or educational equivalent
  • At least 18 months of on-site monitoring experience, ideally including experience monitoring clinical trials in Australia or New Zealand
  • The ability to work independently in a home based environment, with minimal supervision.

Experience monitoring Oncology clinical trials will be highly regarded.

If you want to make an impact in the global research market, where we are working to make a real difference in patient health, we ask you to apply now and join our team.

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Quintiles is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential.

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