I am working with a CRO which is looking for a Senior Clinical Research Associate to expand their team in Sweden.
Perform on-site monitoring visits as well as site identification, feasibility and selection as required
Responsible for evaluating, initiating, monitoring and closing out clinical study sites
Ensure clinical projects are conducted, recorded, and reported in accordance with the project protocol
Comply with Good Clinical Practice (GCP), Company SOPs and all applicable regulatory requirements
Provide ongoing updates and support to project management
At least 2 years of experience as a Clinical Research Associate in Sweden
Multiple experience in therapeutic areas, general medicine would be a bonus
Excellent knowledge of ICH-GCP and any other relevant, local regulatory requirements
Ability to travel 50% of the time
Fluent in English and Swedish
If you’re interested in this role, please get in touch and I will be happy to discuss this in further detail: email@example.com / +44 1273 952187.
Salary: On application
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