Clinical Research Associate II
Core
Monitor Phase I–III clinical trials to ensure compliance with ICH-GCP and regulatory requirements, managing studies across multiple therapeutic areas in France.
Role type
Clinical Research Associate II (CRA II)
Builds
Clinical trial monitoring activities for major global pharmaceutical sponsors
Domain
Healthcare / Clinical Research / Big Pharma
Deliverable
client delivery
Required skills
Clinical trial monitoring, site qualification and management, protocol compliance, data integrity management, regulatory submission management, therapeutic area knowledge (Oncology, Neurology, Psychiatry, Cardiology, Dermatology), clinical trial software proficiency
Preferred skills
Advanced degree in life sciences, nursing, or medicine, experience in CRO or pharmaceutical industry, ability to manage multiple sites and projects simultaneously
Technologies
Clinical trial software and tools
Responsibilities
Conduct site qualification, initiation, monitoring, and close-out visits; Perform data review and resolution of queries; Collaborate with investigators and site staff; Prepare and review study documentation including protocols and clinical study reports; Ensure study cost efficiency and timely issue resolution
Seniority
Mid-level IC
