Senior Clinical Research Associate (Scra)

Covance

Job Overview

We are seeking an exceptional Senior Clinical Research Associate to join our extraordinary people in our clinical operations team that monitors Phase I - IV clinical trials.

Covance Senior Clinical Research Associates:

  • Lead all aspects of study site monitoring according to Covance/Chiltern SOP, 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.

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.

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.

You will join like-minded collaborative professionals at Covance who, together, build our reputation as one of the world's largest and most respected contract research organizations. In choosing Covance, you will be part of a dedicated team that makes a difference in helping to deliver life-saving and life-enhancing medicines to people around the world.

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

  • University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure),

AND 

  • a minimum of 4 years of Clinical Monitoring
  • In lieu of the above education requirement, external candidates with a minimum of 6 years recent clinical monitoring experience will be considered

Experience

  • Have a full understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
  • Advanced site monitoring skills
  • Advanced study site management skills
  • Advanced registry administration skills
  • Ability to work with minimal supervision
  • Good planning and organization skills
  • Ability to resolve project-related problems and prioritizes workload for self and team
  • Ability to work within a project team
  • Works efficiently and effectively in a matrix environment
  • Valid Driver's License

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Why Grow Your Career with Covance?

Covance, the drug development business of LabCorp, is recognized as a leader in drug development because of our exceptional people. At Covance, we embrace and celebrate the different strengths, experiences and perspectives of our 20,000+ team members across the globe. Our team is driven by an energizing purpose to improve health and improve lives. Here, you can play a role in bringing new scientific discoveries to life and make a difference in the lives of millions. And, with our comprehensive service portfolio, you’ll have the opportunity to explore diverse projects and unique career paths across the drug development spectrum. Join us and discover your extraordinary potential.

From FORTUNE. (c)2019 Fortune Media IP Limited. All rights reserved. Used under license. FORTUNE and The World's Most Admired Companies are registered trademarks of Fortune Media IP Limited and are used under license. FORTUNE and Fortune Media IP Limited are not affiliated with, and do not endorse products of, Laboratory Corporation of America Holdings. 

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