CRA - France

​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