Covance

  • Clinical Research Associate / Home-Based or Office-Based

    Job Location(s) NL-Amsterdam
    Job Number
    2018-25662
    Job Category
    Clinical Research Associate
    Position Type
    Full-Time
  • Job Overview

    Seize now the opportunity to join our Clinical Operations team in the Netherlands! Covance is hiring CRAs to be office-based in our offices in Leiden or Home-Based in the Netherlands. 

     

    Covance is known fot is values to strive for operational and service excellence through a relentless focus on People, Process and Clients. 

     

    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.

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