Clinical Research Associate at Covance

Your responsibilities as a CRA would be as follows:

  • Assure the implementation of project plans as assigned
  • Site administration and site monitoring responsibility for clinical studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP
  • Site management responsibility for clinical studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP
  • Act in the project role of as Local Project Coordinator or Lead CRA as assigned

Requirements:

  • Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
  • Have a full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
  • Good planning, organization and problem solving abilities
  • Ability to work with minimal supervision
  • Good communication and interpersonal skills
  • Good analytical and negotiation skills
  • Computer competency
  • Fluent in local office language and in English, both written and verbal
  • Works efficiently and effectively in a matrix environment

We are looking for energizing CRAs, motivated to be part of a great and supportive team involved on the most innovative projects of our times in several therapeutic areas including medical device, oncology, urology... among many others!

As a Covance CRA you will be able to:

  • Thrive in a supportive team environment
  • Enter a role with a clear path for advancement
  • Receive on-the-job training and mentoring if needed or be a mentor to others

Education/Qualifications:

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

Experience:

  • a minimum of 2 years of Clinical Monitoring experience.

Find out more about drug development at Leiden Bio Science Park.

R&D