French-speaking CRA for Global Trials | Part-time UK

Hlx Life Sciences; Wakefield; On-site; GBP 55,000 - 83,000; 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 support sites in a global clinical trial, with emphasis on international studies and, ideally, experience in France.

You will conduct site initiation, monitoring visits, and close-out activities, manage relationships with investigators, ensure protocol and ICH-GCP compliance, and contribute to study documentation with timely reporting.

Qualifications

• Strong independent CRA and site monitoring experience.
• Fluent in French and English.
• UK based with the ability to travel for site visits when required.
• Experience on global/multinational clinical trials.
• Experience monitoring or supporting sites in France is a plus.
• Familiar with ICH-GCP and regional regulations.

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 contact for investigators
• Monitoring recruitment, data quality, site performance and study metrics
• Identifying and escalating site risks and supporting issue resolution
• Ensuring compliance with protocol, ICH-GCP and local regulations
• Reviewing source documentation and site files
• Supporting start-up and activation activities
• Completing monitoring reports within timelines

Skills

Site monitoring

French & English

UK travel

Global trials experience

GCP/regulatory knowledge

Therapy area experience

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 support sites in a global clinical trial, with emphasis on international studies and, ideally, experience in France.

You will conduct site initiation, monitoring visits, and close-out activities, manage relationships with investigators, ensure protocol and ICH-GCP compliance, and contribute to study documentation with timely reporting.