Remote Clinical Trial Operations Manager

Resilience Care; Rennes; Remote; EUR 55,000 - 85,000; Full time

Benefits offered by this job

Fully remote within France

Regular travel

Job summary

Resilience Care, a forward‑looking French company specializing in remote medical monitoring, seeks a Clinical Operations Coordinator to oversee multi-site studies across therapeutic areas. You will report to the Clinical Operations Lead and blend hands-on site oversight with regulatory coordination.

You will ensure data quality, maintain regulatory documentation, and support budget tracking while collaborating with Clinical Scientists, Biostatistics and Product teams.

Qualifications

• Degree in life sciences, pharmacy, clinical research or biomedical engineering.
• At least two years of experience in clinical research (e.g., CRA, site manager, or junior PM).
• Experience in operational follow-up of clinical sites or studies.
• Ability to work in French and English with professional fluency.

Responsibilities

• Coordinate day-to-day study operations and logistics, and support site selection, initiation, monitoring and close-out visits.
• Track site progress, study indicators and data quality; share issues during governance meetings.
• Follow up on site agreements, amendments and budget annexes; contribute to site budget tracking and payment follow-up with Legal and Finance.
• Maintain regulatory documentation and the eTMF; support audit readiness and ensure compliance with GCP, ICH guidelines, the French Jardé Law and GDPR.
• Work with Clinical Scientists, Biostatistics and Product teams to improve clinical operations trackers and SOPs.

Skills

Study coordination

GCP / ICH / GDPR

Documentation management

Regulatory submission

Cross-functional communication

Education

Degree in life sciences, pharmacy, clinical research or biomedical engineering

Job description

Resilience Care, a forward‑looking French company specializing in remote medical monitoring, seeks a Clinical Operations Coordinator to oversee multi-site studies across therapeutic areas. You will report to the Clinical Operations Lead and blend hands-on site oversight with regulatory coordination.

You will ensure data quality, maintain regulatory documentation, and support budget tracking while collaborating with Clinical Scientists, Biostatistics and Product teams.