CRA (Paris, Lyon & Nantes)
Core
Clinical monitoring and site management for clinical trials, ensuring protocol and regulatory compliance 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
Deliverable
client delivery
Required skills
Clinical monitoring, site management, ICH-GCP guidelines, Risk Based Monitoring, medical terminology, travel management, documentation handling
Preferred skills
Life sciences degree, Registered Nursing certification, Microsoft Office proficiency
Technologies
Microsoft Office
Responsibilities
Coordinate clinical monitoring and site management processes, conduct remote or on-site site visits, manage procedures from various sponsors, develop relationships with investigational sites, ensure audit/inspection readiness
Seniority
Entry-level to Mid-level, hands-on IC