Covance

  • Senior CRA - Sweden

    Job Location(s) SE | SE-AB-Stockholm
    Job Number
    2018-22115
    Job Category
    Clinical Research Associate
    Position Type
    Full-Time
  • Job Overview

    Covance is searching for a Senior CRA in Sweden to monitor trials mainly within Oncology and Cardiology diseases.

     

    This role is 100% SPONSOR dedicated with a prestigeous Pharmaceutical company so there will be no working across multiple SOPs!!

     

    What makes this opportunity special?

     

    • Career progression will be exceptional because there are lots of studies coming through in 2018 across a variety of therapeutic areas
    • We offer lots of flexibility with great opportunity to progress into a variety of areas such as Project Manager, CTL, Line Manager, SSU Manager and cross boarder roles in the future.
    • The working conditions within our Swedish team is great! A very positive environment where everyone works together well and in harmony.
    • The job is permanent, full time & 100% home-based OR office based in Stockholm.
    • You will be joining a large team with a well organised structure and robust processes in place
    • Competitive salary, car allowance and benefits package, including lunch vouchers
    • There will be no formal contractual expectations regarding frequency of visits

    Education / Qualifications

    • University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)
    • In lieu of the above requirement, candidates with three (3) or more years of relevant clinical research experience in pharmaceutical or CRO industries may be considered
    • Fluent in Swedish and English

    Experience

    • Minimum of four (4) years of clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits).
    • In lieu of the above requirements, candidates with > five (5) years supervisory experience in a health care setting and three (3) years clinical research experience in the pharmaceutical or CRO industries (including monitoring) will be considered.
    • Have a full understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs.
    • Excellent site monitoring skills.
    • Excellent study site management skills.

    Options

    Sorry the Share function is not working properly at this moment. Please refresh the page and try again later.
    Share on your newsfeed

    Tell Us About Yourself

    Not ready to apply? Connect with us to join our talent community.