French-speaking Clinical Research Associate

Hlx Life Sciences; Aberdeen City; Sur place; GBP 40 000 - 50 000; Temps partiel

Résumé du poste

Freelance CRA – UK role on a part-time, sponsor-dedicated project. Based in the UK, you will monitor sites, conduct initiation, routine monitoring and close-out visits, and coordinate with investigators and cross-functional teams across international studies.

The ideal candidate is fluent in French and English, has strong independent CRA experience, can travel for site visits, and understands ICH-GCP and local regulations. Oncology/rare disease experience preferred.

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.

Responsabilités

• 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

Connaissances

CRA experience

Site monitoring

French language

English language

UK-based travel

Description du poste

Freelance CRA – UK | French & English Speaking

I’m currently supporting a CRO looking to bring an experienced Freelance CRA onto a part-time, sponsor-dedicated project.

The CRA will be based in the UK and work closely with both the CRO and sponsor teams, supporting sites as part of a global clinical trial. We’re particularly interested in CRAs who have experience working across international studies and ideally have previously supported sites in France.

Key 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

Experience required:

• 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 working on global/multinational clinical trials
• Previous experience monitoring or supporting clinical trial sites in France would be ideal
• Comfortable working across international and cross-functional study teams
• Strong knowledge of ICH-GCP and clinical trial regulations
• Oncology, Rare Disease and/or Neurology experience preferred

Contract details:

• Freelance / contract
• Part-time
• UK based
• Global clinical trial
• Site travel required