French-Speaking Freelance CRA for Global UK Trials

Hlx Life Sciences; Woking; On-site; GBP 55,000 - 103,000; Part time

Job summary

HLX Life Sciences is seeking a Freelance CRA in the UK to join a sponsor-dedicated, part-time project. You will monitor sites across international trials, initiate sites, conduct routine monitoring, and manage relationships with investigators and site teams.

Travel to sites in France and other regions may be required. The role requires strong independent CRA experience, fluency in French and English, and familiarity with ICH-GCP regulations.

Qualifications

• Strong independent CRA and site monitoring experience.
• Fluent in French and English.
• UK based with ability to travel for site visits when required.
• 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

CR A monitoring

Site coordination

ICH-GCP knowledge

French & English fluency

Travel readiness

Global trials experience

Job description

HLX Life Sciences is seeking a Freelance CRA in the UK to join a sponsor-dedicated, part-time project. You will monitor sites across international trials, initiate sites, conduct routine monitoring, and manage relationships with investigators and site teams.

Travel to sites in France and other regions may be required. The role requires strong independent CRA experience, fluency in French and English, and familiarity with ICH-GCP regulations.