I am looking for a CRA based in France to work on across a number of different projects for a global CRO.
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
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: email@example.com /+44 1273 952187.
Salary: On application
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