Part-Time French-Speaking CRA for Global Trials (UK)

Hlx Life Sciences; South Shields; On-site; GBP 32,000 - 42,000; Part time

Job summary

HLX Life Sciences is seeking a Freelance CRA in the United Kingdom for a part-time, sponsor-dedicated project. The candidate will monitor sites within a global clinical trial, with potential involvement across international sites and France.

The role requires strong independent CRA experience, fluency in French and English, and willingness to travel for site visits. Experience in oncology, rare disease, or neurology is preferred.

Qualifications

• Strong independent CRA and site monitoring experience.
• Fluent in French and English.
• UK based with the 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

Independent CRA

Site Monitoring

Bilingual FR/EN

Job description

HLX Life Sciences is seeking a Freelance CRA in the United Kingdom for a part-time, sponsor-dedicated project. The candidate will monitor sites within a global clinical trial, with potential involvement across international sites and France.

The role requires strong independent CRA experience, fluency in French and English, and willingness to travel for site visits. Experience in oncology, rare disease, or neurology is preferred.