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CRA I/II/ Sr CRA - FSP - UK

💼 Full-time🗓 2026-09-16 → 2026-09-26

Core

Conduct independent on-site clinical monitoring to ensure quality and accuracy of clinical trial data across multi-national projects.

Role type

Senior IC Clinical Research Associate (CRA)

Builds

Clinical trial monitoring activities for pharmaceutical and clinical research organization clients

Domain

Life sciences / Clinical research / Pharmaceutical

Deliverable

client delivery

Required skills

ICH-GCP compliance, EU and FDA regulatory requirements, medical/therapeutic area knowledge, medical terminology, independent on-site monitoring

Preferred skills

multi-national project team collaboration, collegiate environment ownership

Technologies

clinical trial management systems (implied by context of monitoring activities)

Responsibilities

Perform and coordinate all aspects of the clinical monitoring process; conduct monitoring activities independently; deliver exemplary customer service on challenging projects

Seniority

Mid-level to Senior, hands-on IC

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