Senior CRA — Independent Site Monitor | Flexible Hours

Allucent; Paris; Hybride; EUR 52 000 - 72 000; Plein temps

Avantages offerts par ce poste

Comprehensive benefits

Competitive salary

Training budget

Flexible hours

Buddy Program

Growth opportunities

Referral program

Loyalty awards

Résumé du poste

Allucent is seeking a Clinical Research Associate (CRA) to independently monitor investigational sites across study phases in France. You will lead monitoring activities, ensure protocol and regulatory compliance, and maintain trial integrity with a collaborative team.

You’ll manage site relationships and support regulatory affairs and study startup processes. The role requires 2+ years of monitoring experience, strong ICH-GCP knowledge, bilingual English/French communication, independence, and

Qualifications

• Experience leading monitoring activities in complex trials with a minimum of 2 years.
• Strong understanding of ICH-GCP and regulatory guidelines.
• Clear and confident communicator in English and French.
• Comfortable working independently and managing priorities.
• Willingness to travel, as required (8 DOS per month).

Responsabilités

• Independently manage all aspects of monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and close-out visits.
• Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements.
• Build strong site relationships, acting as a primary point of contact and ensuring high-quality data collection.
• Identify and resolve site issues, escalating as needed to maintain trial integrity and patient safety.
• Activities around regulatory affairs, site activation and study-startup.

Connaissances

English

French

Description du poste

Allucent is seeking a Clinical Research Associate (CRA) to independently monitor investigational sites across study phases in France. You will lead monitoring activities, ensure protocol and regulatory compliance, and maintain trial integrity with a collaborative team.

You’ll manage site relationships and support regulatory affairs and study startup processes. The role requires 2+ years of monitoring experience, strong ICH-GCP knowledge, bilingual English/French communication, independence, and