Remote Clinical Trials Manager

Resilience Care; Paris; Remote; EUR 70,000 - 90,000; Full time

Job summary

Resilience Care is seeking a Clinical Operations professional to coordinate studies sponsored by Resilience and investigator-initiated across multiple therapeutic areas. You will report to a Clinical Operations Lead, combining hands-on site oversight with regulatory and contractual coordination.

You will ensure study documentation quality, data integrity, and smooth operation of regulatory processes while collaborating with cross-functional teams.

Qualifications

• You know how to organize clinical study activities and track priorities, deadlines and actions across stakeholders.
• You apply GCP and the relevant requirements of ICH guidelines, the French Jardé Law and GDPR.
• You maintain structured study documentation and use study indicators to monitor progress.
• You contribute to regulatory submission follow-up, site contracting and budget tracking.
• You work in French and English with professional fluency, both written and spoken.

Responsibilities

• Coordinate day-to-day study operations and logistics, including site selection, initiation, monitoring and close-out visits.
• Track site progress and data quality; report issues in governance meetings.
• Follow up on site agreements, amendments and budget annexes; assist with payments.
• Maintain regulatory documentation and the eTMF; support audit readiness and compliance with GCP, ICH, Jardé Law and GDPR.
• Collaborate with Clinical Scientists, Biostatistics and Product teams; improve operations trackers and SOPs.

Skills

Study coordination

GCP & ICH

Documentation management

Regulatory submission

Bilingual FR/EN

Education

Life sciences / pharmacy / clinical research

Job description

Resilience Care is seeking a Clinical Operations professional to coordinate studies sponsored by Resilience and investigator-initiated across multiple therapeutic areas. You will report to a Clinical Operations Lead, combining hands-on site oversight with regulatory and contractual coordination.

You will ensure study documentation quality, data integrity, and smooth operation of regulatory processes while collaborating with cross-functional teams.