French-Speaking CRA for Global Trials | UK-Based, Part-Time

Hlx Life Sciences; Warrington; On-site; GBP 40,000 - 60,000; Part time

Job summary

HLX Life Sciences is seeking an experienced Freelance CRA in the United Kingdom to support a sponsor-dedicated, part-time trial. The role requires fluent French and English and UK-based travel to sites across a global study.

You will conduct site initiation, routine monitoring and close-out visits, manage site relationships, and ensure data quality and regulatory compliance across international sites. Prior experience with multinational trials and oncology/rare disease/neurology is preferred.

Qualifications

• Strong independent CRA and site monitoring experience.
• UK based with ability to travel for site visits.
• Experience working on global/multinational clinical trials.
• 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

CRA monitoring

Bilingual French/English

Job description

HLX Life Sciences is seeking an experienced Freelance CRA in the United Kingdom to support a sponsor-dedicated, part-time trial. The role requires fluent French and English and UK-based travel to sites across a global study.

You will conduct site initiation, routine monitoring and close-out visits, manage site relationships, and ensure data quality and regulatory compliance across international sites. Prior experience with multinational trials and oncology/rare disease/neurology is preferred.