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

Hlx Life Sciences; Doncaster; On-site; GBP 65,000 - 101,000; Part time

Job summary

HLX Life Sciences is seeking a Freelance CRA in the UK for a part-time, sponsor-dedicated project. You will manage monitoring activities across assigned clinical trial sites and conduct site initiation, routine monitoring, and close-out visits.

The role requires fluent French and English, UK base with travel for site visits, and experience in global/multinational trials. Monitoring or supporting sites in France is a plus.

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 on global/multinational clinical trials.
• Ideal: monitoring or supporting sites in France.
• Comfortable working across international study teams.
• Solid knowledge of ICH-GCP and 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 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 (French/English)

Global/multinational trials

Travel readiness

Job description

HLX Life Sciences is seeking a Freelance CRA in the UK for a part-time, sponsor-dedicated project. You will manage monitoring activities across assigned clinical trial sites and conduct site initiation, routine monitoring, and close-out visits.

The role requires fluent French and English, UK base with travel for site visits, and experience in global/multinational trials. Monitoring or supporting sites in France is a plus.