Are you an organized person who can work independently and take ownership of your career? Would you like to gain on-the-job skills while helping advance life-changing medicines?
If you are looking to enter a nurturing environment that provides a clear path to advancement, consider furthering your career as a Covance Clinical Research Associate (CRA). In this role, you will:
-University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure)
- A minimum of six months on-site monitoring (preferred).
-Internal candidates with a minimum of 6 months of experience as a Clinical Research Assistant
-Internal candidates with a minimum 2 years clinical trials or site management experience (e.g. study coordinator, project coordinator, project specialist, study start- up)
-Basic understanding of ICH Guidelines and GCP including a basic understanding of regulatory requirements
-Basic understanding of the clinical trial process
-Valid Driver’s License
Working knowledge of Covance SOPs for site monitoring
o a minimum of six months of on-site monitoring (preferred)
o Internal candidates with a minimum 2 years clinical trials or site management experience (e.g. study coordinator, project coordinator, project specialist, study start-up)