Senior Clinical Research Associate I (SCRA)
covance
Melbourne, Australia
1d ago

Job Overview :

Are you ready to discover your career potential with Covance?

We are seeking exceptional Clinical Research Associates (CRAs) to join our growing Clinical FSPx team in Australia.

Allocated to a global pharmaceutical company who has an outstanding reputation for recognizing their employees, you will enjoy working on one set of SOPs, monitoring sites across Australia and have the flexibility to work from home.

You will also be employed permanently by Covance giving you the best of both worlds to develop and broaden your career across our exceptional company.

So if you are passionate about Clinical Research and a person who has experience independently monitoring Phase I - IV clinical study sites in Australia, let’s talk as we may have a job for you.

As a Clinical Research Associate at Covance you will :

  • Lead all aspects of study site monitoring according to Client SOPs, GCP, and ICH guidelines
  • Partner with investigators and study coordinators on pre-study qualification and site initiation visits
  • Conduct routine study site monitoring visits
  • Close-out clinical sites, and ensure study files are up to date to maintain the success of the study.
  • Covance Australia is committed to providing you the flexibility to work from home, the freedom to grow & develop your career across all phases and areas of clinical trial operations, as well as provide state of the art technology and processes that help to give you time back to enjoy family life.

    Discover your potential in a company that truly invests in you. Talk to us to learn more and explore your career. Apply online today.

    We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

    Education / Qualifications :

  • Life Science Degree or RN qualified
  • Experience :

  • Ideally Three (3) years of independent clinical site monitoring experience
  • Excellent knowledge of ICH-GCP and SAE reporting
  • Great communication skills
  • Available to travel interstate across Australia to attend study site visits
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