​CRA

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

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Requirements:

• At least 2 years of experience as a Clinical Research Associate

• 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 Polish

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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

Salary: On application