Covance is currently looking for a Senior CRA in the Stockholm or Uppsala area of Sweden to monitor trials mainly within Oncology (Prostate, bladder, head & neck, breast and Lymphoma). This is a client dedicated role with a top 10 Pharma company and so you will only be working to a single set of SOPs

To qualify you NEED at least 2 years of CRA experience in Sweden but ideally 2-3 years and you MUST have worked on Oncology trials previously. In addition it would be advantageous if have done some 'recist' training.

Why apply for this job!?:

• Career progression will be exceptional because there are lots of studies coming through in 2019 across a variety of therapeutic areas
• Your Line Manager will also be based in Sweden (Stockholm)
• 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. You can also become a Therapy area expert if you are scientifically strong.
• 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.
• If you want to be office based in Stockholm then you can; the option is available
• 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

Other Information:
For more information please contact Andy Smith at Covance on +44 (0)7775 848 250 or mail andy.smith@covance.com

Key words:

Oncology, Sweden, Stockholm, Uppsala, CRA Clinical Research Associate, Monitor

REMOTE
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 proven relevant clinical research experience in pharmaceutical or CRO industries may be considered

Experience:

• Solid experience of Monitoring clinical trials in Sweden
• Fluency in English and Swedish