France-based CRA | Travel & Flexible Hours

Allucent; Paris (TX); On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

Benefits package

Competitive salary

Training budget

Flexible hours

Buddy program

Career growth

Referral program

Spot bonus

Loyalty awards

Job summary

Allucent is seeking a Clinical Research Associate (CRA) to lead monitoring activities, own site relationships, and bridge sponsor-site communications to ensure trial integrity. The role includes regulatory and startup tasks with travel across France, requiring fluency in English and French and independent work with strong prioritization.

Candidate should have at least 2 years of monitoring experience, knowledge of ICH-GCP, and a flexible, proactive approach to study-startup and site activation

Qualifications

• Experience leading monitoring activities in clinical trials (min 2 years).
• Strong understanding of ICH-GCP and regulatory guidelines.
• Clear and confident communicator in English and French.
• Independent worker with good prioritization.
• Willingness to travel (8 days per month).

Responsibilities

• Independently manage monitoring for trials across phases, including site initiation, routine monitoring, and close-out visits.
• Ensure compliance with protocols, GCP, ICH, SOPs, and regulatory requirements.
• Build strong site relationships as primary contact and ensure high-quality data.
• Identify and resolve site issues, escalating to maintain trial integrity and patient safety.
• Contribute to regulatory affairs, site activation and study-startup activities.

Skills

Monitoring

Site relationships

Travel readiness

Communication

Job description

Allucent is seeking a Clinical Research Associate (CRA) to lead monitoring activities, own site relationships, and bridge sponsor-site communications to ensure trial integrity. The role includes regulatory and startup tasks with travel across France, requiring fluency in English and French and independent work with strong prioritization.

Candidate should have at least 2 years of monitoring experience, knowledge of ICH-GCP, and a flexible, proactive approach to study-startup and site activation