Freelance Clinical Research Associate (CRA)

• Manage and monitor clinical studies
• Conduct site initiation, pharmacy monitoring, and site close-out visits in accordance with the protocol
• Record and track patient enrollment
• Verify the quality of data recorded in case report forms (CRFs)
• Answer investigators’ questions
• Prepare information letters
• Write monitoring reports and follow-up letters
• Comply with applicable regulations, Good Clinical Practice (GCP), and current procedures

Requirements

• Advanced degree or training in clinical research
• Senior Clinical Research Associate (CRA) profile only
• Freelance assignment
• Ideally, 5 years of operational monitoring experience as a Clinical Research Associate in a public- or private-sector environment
• Fluency in French
• Good professional level of English
• Scientific rigor
• Ability to work independently
• Strong interpersonal skills
• Excellent organizational skills
• Based in Paris or Lyon, with regional and national travel

Core Competencies

Demonstrates expertise in managing and monitoring clinical studies, ensuring compliance with Good Clinical Practice (GCP) and applicable regulations. Proficient in patient enrollment tracking, data verification, and effective communication with investigators.

Highest-signal resume keywords

• Clinical Research Management
• Operational Monitoring Experience
• Good Clinical Practice (GCP)
• Fluency in French
• Excellent Organizational Skills

ATS Optimization Keywords

Hard Skills

• Clinical Study Management
• Data Verification
• Patient Enrollment Tracking
• Monitoring Report Writing
• Site Initiation
• Pharmacy Monitoring
• Site Close-Out Visits
• Regulatory Compliance
• Case Report Form (CRF) Review
• Scientific Rigor

Soft Skills

• Strong Interpersonal Skills
• Ability to Work Independently

Certifications & Qualifications

• Advanced Degree in Clinical Research

Industry Keywords

• Clinical Research Associate (CRA)
• Public Sector
• Private Sector
• Freelance Assignment
• Regional and National Travel