Clinical Research Associate - Sweden

I am working with a CRO which is looking for a Senior Clinical Research Associate to expand their team in Sweden.

Responsibilities:

• 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

Requirements:

• 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: roxanna.keshavarz@rbwconsulting.com / +44 1273 952187