Freelance Clinical Research Associate

I am partnered with a small, niche CRO which is looking for a Freelance Clinical Research Associate based in Poland for 1 FTE over a 6 or 12 month contract.

Responsibilities:

• Perform on-site monitoring visits as well as site identification, feasibility and selection as required
• Assist in the preparation and management of regulatory and ethics applications for clinical research studies as required
• Prepare project-specific support materials and templates in accordance with protocol and other specifications
• Manage the content of project site-level Trial Master Files and ensure accuracy and completeness

Requirements:

• Background in multiple therapeutic areas
• Driving Licence with ability to travel to sites when needed
• Fluent in Polish and English
• Independent monitoring experience of a minimum of 2 years needed
• Experience with regulatory and ethics submissions across clinical trials

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 or +44 1273 952187