Experienced Clinical Research Associate
Core
Conducting clinical monitoring visits and ensuring data compliance for research sites in France.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance for biopharma projects
Domain
Clinical Research / Biopharmaceuticals
Deliverable
client delivery
Required skills
Clinical monitoring, GCP compliance, Adverse event reporting, Site qualification, Protocol adherence, Patient recruitment assessment, Documentation management, Regulatory document review
Preferred skills
CRA lead experience, Mentoring, SME role, Transversal activity
Technologies
CTMS, Microsoft Office
Responsibilities
Conduct qualification, initiation, monitoring, and closeout visits; Verify adverse events and data accuracy; Assess patient recruitment and retention; Ensure GCP and SOP compliance; Complete monitoring reports and follow-up letters.
Seniority
Experienced IC
