Clinical Research Associate II – Sr Clinical Research Associate

Jobtailor; Paris; Sur place; EUR 42 000 - 64 000; Plein temps

Résumé du poste

Jobtailor in Paris seeks an experienced Clinical Research Associate to independently monitor assigned trials, across study phases, ensuring data quality and regulatory compliance. You will build strong site relationships, act as a primary contact, and collaborate with the team to maintain trial integrity.

The role requires 2+ years as an independent site monitor, fluency in English and French, and willingness to travel within France. Oncology/rare disease monitoring experience is a plus.

Qualifications

• Minimum 2 years’ experience as independent site monitor.
• Strong understanding of ICH-GCP and regulatory guidelines.
• Proficient in English and French.
• Able to travel within France.
• Experience in oncology or rare disease monitoring is a plus.

Responsabilités

• Independently manage monitoring across all study phases.
• Ensure protocol and regulatory compliance (GCP, ICH).
• Build strong site relationships and ensure high-quality data collection.
• Identify and resolve site issues to maintain trial integrity and patient safety.
• Mentor and support junior CRAs.

Connaissances

Independent site monitoring

Clinical monitoring

English and French communication

Description du poste

Responsibilities

• 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.
• Mentor and support junior CRAs, sharing knowledge and best practices.

Requirements

• Experience leading monitoring activities in complex trials, ideally in oncology or rare disease with a minimum of 2 years’ experience as independent site monitor
• 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 in France, as required.