CRA (Paris & Lyon)
Core
Clinical monitoring and site management for clinical trials, ensuring protocol compliance and data reliability across commercial and government contracts.
Role type
Clinical Research Associate (CRA)
Builds
End-to-end clinical trial programs for pharma/biotech clients
Domain
Clinical Research / Life Sciences
Required skills
Clinical monitoring, ICH-GCP guidelines, Regulatory compliance, Site management, Risk Based Monitoring, Medical terminology, Time management, Microsoft Office, Travel management, Documentation handling
Preferred skills
Life sciences degree, Registered Nursing certification, French language fluency, English language fluency, Therapeutic area knowledge
Technologies
Microsoft Office, Clinical trial software
Responsibilities
Conduct remote or on-site site visits to assess protocol and regulatory compliance, Manage procedures and guidelines from different sponsors, Develop collaborative relationships with investigational sites, Ensure audit and inspection readiness, Coordinate all aspects of the clinical monitoring process
Seniority
Entry-level to Mid-level, hands-on IC