Clinical Research Associate - France

As the needs for clinical trials are rapidly increasing across Europe, one of my clients in the CRO sector are looking to once again expand their clinical team across France.

I am looking for a CRA to work on a project for a large CRO dedicated to one sponsor across, predominantly, oncology studies.

As a CRA, you will be working from home and travelling to sites localised to your region.

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:

• Strong experience across multiple therapeutic areas
• Previous experience working with pharmaceutical/biotech companies or CROs
• Independent monitoring experience of a minimum of 2 years needed
• Driving Licence with ability to travel to sites when needed
• Fluent in French and English
• Experience with regulatory and ethics submissions across clinical trials

Ideally, the client would prefer you to be working from their office in France for 2 days a week but this could potentially be negotiable depending on your experience,

If you’re interested in this role, please get in touch and I will be happy to discuss this in further detail:

?+44 1273 952187

? roxanna.keshavarz@rbwconsulting.com