Freelance French-Speaking CRA for Global Trials

Hlx Life Sciences; Birmingham; On-site; GBP 45,000 - 65,000; Part time

Job summary

HLX Life Sciences is seeking an experienced Freelance CRA for a part-time, sponsor-dedicated project based in the United Kingdom. You will monitor sites across a global trial, support initiation visits, and maintain strong Investigator relationships while navigating France sites when required.

The role requires fluent French and English, UK-based with travel for site visits, and experience in multinational trials. ICH-GCP knowledge and cross-functional collaboration are essential.

Qualifications

• Strong independent CRA and site monitoring experience.
• Fluency in French and English required.
• UK-based with travel for site visits.
• Experience on global/multinational clinical trials.
• France site monitoring experience is a plus.
• Comfortable working across cross-functional study teams.
• Solid knowledge of ICH-GCP and trial regulations.
• Oncology, Rare Disease or Neurology experience preferred.

Responsibilities

• Managing monitoring activities across assigned clinical trial sites
• Conducting site initiation, routine monitoring and close-out visits
• Maintaining site relationships and acting as a key 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

Fluent French

Fluent English

Independent CRA experience

UK based

Multinational trials

Job description

HLX Life Sciences is seeking an experienced Freelance CRA for a part-time, sponsor-dedicated project based in the United Kingdom. You will monitor sites across a global trial, support initiation visits, and maintain strong Investigator relationships while navigating France sites when required.

The role requires fluent French and English, UK-based with travel for site visits, and experience in multinational trials. ICH-GCP knowledge and cross-functional collaboration are essential.