• CRA II / Senior CRA - Sweden

    Job Location(s) SE | SE-AB-Stockholm
    Job Number
    Job Category
    Clinical Research Associates
    Position Type
  • Job Overview

    Covance is searching for a CRA II or 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 2019 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


    • Minimum of two (2) 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.


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