Covance Senior CRA - Sweden in Stockholm, Sweden
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
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.
Job Number 2018-22115
Job Category Clinical Research Associate
Position Type Full-Time
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