CRA (Paris & Lyon)

Thermo Fisher Scientific · Ivry-sur-Seine, France

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Clinical OperationsFull timeCompany career page

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Role summary

Clinical Research Associate role supporting clinical trial operations across Paris and Lyon. Responsibilities include site monitoring, protocol compliance verification, and collaborative relationship management with investigational sites to ensure trial integrity and regulatory adherence.

What they're looking for

Bachelor's degree in life sciences, nursing certification, or equivalent education and experience
Minimum one year of clinical monitoring experience
Fluent in French and English, both written and oral communication
Valid driver's license with ability to travel eight days monthly on-site
Strong understanding of ICH-GCP guidelines and applicable regulations
Proficiency with Microsoft Office and willingness to learn trial management software
Medical/therapeutic area knowledge and attention to detail

What you'll be doing

Conduct remote and on-site monitoring visits to assess protocol compliance and regulatory adherence
Manage documentation and site procedures across various sponsor and monitoring environments
Build and maintain collaborative relationships with investigational sites throughout trials
Ensure audit and inspection readiness through consistent monitoring and documentation
Apply risk-based monitoring concepts to support trial conduct per ICH-GCP standards

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