Covance

  • (Senior) Clinical Research Associate, Netherlands

    Job Location(s) NL-Amsterdam
    Job Number
    2018-18037
    Job Category
    Clinical Research Associate
    Position Type
    Full-Time
  • Job Overview

    We are currently looking for a talented Clinical Research Associates to join our Clinical Operations team in Netherlands. You will have an opportunity to work on different projects for different sponsors within this department.

     

    You will become a part of our team who is always ready to help. We offer a home based position so you will not spend time on unnecessary travels but at the same time we highlight a true live relationship between colleagues. You will have a possibility to devote all your professional skills and knowledge into monitoring investigational sites as we organize our work environment and responsibilities with high standards.

     

    Responsibilities include:

     

    • All details of site management as prescribed in the project plans
    • Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks
    • Negotiation of study budgets with potential investigators and cooperation with Covance legal department with statements of agreements
    • Serious Adverse Event (SAE) reporting, production of reports, narratives and follow up of SAEs.
    • Case Report Forms (CRF) review; query generation and resolution against established data review guidelines on Covance or client data management systems

    Education / Qualifications

    Educational background in life sciences

    Experience

    • Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
    • Excellent understanding of Serious Adverse Event (SAE) reporting
    • Ability to resolve project-related problems and prioritize workload for self and team
    • You have previous clinical research monitoring Experience (including pre-study, initiation, routine monitoring and closeout visits).

    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.

     

    Key words:

     

    Clinical Research, CRA II, Clinical Research Associate, Netherlands, Monitor, Monitoring, Senior Clinical Research Associate, CRA I, Field Based, Home Based, CRO, Pharmaceutical, CRA

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