French-Speaking Freelance CRA for Global UK Trials

Hlx Life Sciences; Cardiff; On-site; GBP 55,000 - 83,000; Part time

Job summary

Hlx Life Sciences is seeking an experienced Freelance CRA for a part-time UK-based role supporting a sponsor and global trial activities, including site monitoring, initiation visits, and close-out visits.

The successful candidate will work across international studies, interact with investigators, ensure ICH-GCP compliance, and coordinate with cross-functional teams; French and English fluency is required.

Travel to sites in the UK and abroad is expected as needed.

Qualifications

• Extensive independent CRA and site monitoring experience.
• Fluent in French and English.
• UK based with ability to travel for site visits.
• Experience working on global/multinational clinical trials.
• Experience monitoring or supporting sites in France is a plus.
• Strong knowledge of ICH-GCP and clinical trial regulations.
• Oncology, Rare Disease and/or Neurology experience preferred.

Responsibilities

• Managing monitoring activities across assigned clinical trial sites
• Conducting site initiation, routine monitoring and close-out visits
• Managing site relationships and acting as a key point of contact for investigators and site teams
• Monitoring recruitment, data quality, site performance and key study metrics
• Identifying and escalating site-level risks and supporting resolution of study issues
• Ensuring compliance with the protocol, ICH-GCP and applicable local regulations
• Reviewing source documentation, study documentation and site files
• Supporting study start-up and site activation activities where required
• Completing monitoring reports and study documentation within agreed timelines

Skills

Site monitoring

Clinical trials

French language

English language

Travel readiness

ICH-GCP knowledge

Cross-functional collaboration

Job description

Hlx Life Sciences is seeking an experienced Freelance CRA for a part-time UK-based role supporting a sponsor and global trial activities, including site monitoring, initiation visits, and close-out visits.

The successful candidate will work across international studies, interact with investigators, ensure ICH-GCP compliance, and coordinate with cross-functional teams; French and English fluency is required.

Travel to sites in the UK and abroad is expected as needed.