Senior Clinical Research Associate

​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