Clinical Research Associate

I am looking for a CRA based in France to work on across a number of different projects for a global CRO.

Responsibilities:

• Perform on-site monitoring visits as well as site identification, feasibility and selection 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
• Assist in the preparation and management of regulatory and ethics applications for clinical research studies as required

Requirements:

• Background across different therapeutic areas
• Previous experience working with pharmaceutical/biotech companies or CROs
• Independent monitoring experience of a minimum of 18 months’
• Driving Licence with ability to travel to sites when needed
• Fluent in French and English
• 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 /+44 1273 952187