CRA I/II/ Sr CRA - FSP - UK
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