​CRA

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

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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

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This position will be client office based in France with 2 home-based days per week.

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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: +44 1273 952187

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Salary: On application