French-Speaking CRA – UK, Part-Time, Global Trials

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

Job summary

Hlx Life Sciences is seeking a Freelance Clinical Research Associate (CRA) for a part-time UK-based project, coordinating with sponsor and CRO teams across international sites on a global clinical trial. The role focuses on site monitoring, initiating visits, and maintaining study documentation.

The ideal candidate is fluent in French and English, brings strong independent CRA experience, and can travel for site visits. Oncology/rare disease/neurology exposure and ICH-GCP knowledge are preferred.

Qualifications

• Fluent in French and English.
• UK-based with ability to travel for site visits.
• Experience in global/multinational clinical trials.
• ICH-GCP knowledge and regulatory familiarity.
• 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

French & English

Independent CRA experience

Travel for site visits

Global multinational trials

Job description

Hlx Life Sciences is seeking a Freelance Clinical Research Associate (CRA) for a part-time UK-based project, coordinating with sponsor and CRO teams across international sites on a global clinical trial. The role focuses on site monitoring, initiating visits, and maintaining study documentation.

The ideal candidate is fluent in French and English, brings strong independent CRA experience, and can travel for site visits. Oncology/rare disease/neurology exposure and ICH-GCP knowledge are preferred.