Senior / Clinical Research Associates

Clinical Research Associate – the role

Whether you’re beginning or continuing your career as a CRA, this role is an ideal stepping-stone. You’ll have training and development to plan and progress your career in the direction you choose. And you won’t do it alone – you’ll have dedicated mentoring and structured quarterly reviews on performance, promotion and bonus awards.

Award winning and innovative, we’ll 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. You’ll be building a smart and flexible career with no limits.

While projects vary, your typical responsibilities might include:

  • 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.

Minimum requirements:

You should have:

  • A Bachelor’s degree or equivalent in a health care or other scientific discipline
  • Successful completion of a CRA Trainee Program or at least three months of on-site monitoring experience
  • Alternatively, you should have an equivalent combination of education, training and experience

If you want to make an impact in a global market, where we are working to make a real difference to patient health, then apply now. You could be the difference.

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