French-Speaking Freelance CRA – UK, Part-Time

Hlx Life Sciences

Warmley

On-site

GBP 42,000 - 65,000

Part time

14 days+
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Job summary

Hlx Life Sciences is seeking an experienced Freelance CRA for a part-time, sponsor-dedicated project in the UK. The role involves supporting global multicentre trials and will require travel to site visits as needed to ensure high-quality data and compliance with study protocols.

Fluency in French and English, strong knowledge of ICH-GCP, and prior monitoring at international sites (ideally in France) are highly valued.

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.
  • 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.

Job description

Hlx Life Sciences is seeking an experienced Freelance CRA for a part-time, sponsor-dedicated project in the UK. The role involves supporting global multicentre trials and will require travel to site visits as needed to ensure high-quality data and compliance with study protocols.

Fluency in French and English, strong knowledge of ICH-GCP, and prior monitoring at international sites (ideally in France) are highly valued.

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