French-speaking Freelance CRA – UK, Global Trials

Hlx Life Sciences; Guildford; On-site; GBP 40,000 - 56,000; Part time

Job summary

Hlx Life Sciences is seeking a freelance CRA for a part-time sponsor-dedicated project in the UK. You will support global clinical trial sites, conducting monitoring, initiation, and close-out visits while collaborating with CRO and sponsor teams.

The role requires fluent French and English, strong ICH-GCP knowledge, and prior experience across multinational trials, including sites in France. UK-based travel is expected, with flexible part-time arrangements on a sponsor-led program.

Qualifications

• Strong independent CRA and site monitoring experience.
• Fluent in French and English.
• UK based with the ability to travel for site visits.
• Experience working on global/multinational clinical trials.
• Previous experience monitoring or supporting clinical trial sites in France would be ideal.
• Comfortable working across international and cross-functional study teams.
• 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

Independent CRA experience

French & English fluency

Travel for site visits

Job description

Hlx Life Sciences is seeking a freelance CRA for a part-time sponsor-dedicated project in the UK. You will support global clinical trial sites, conducting monitoring, initiation, and close-out visits while collaborating with CRO and sponsor teams.

The role requires fluent French and English, strong ICH-GCP knowledge, and prior experience across multinational trials, including sites in France. UK-based travel is expected, with flexible part-time arrangements on a sponsor-led program.