CRA I/II/ Sr CRA - FSP - UK
Core
Conduct independent on-site clinical monitoring to ensure data quality and regulatory compliance for pharmaceutical clinical trials.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory adherence for pharmaceutical clients
Domain
Life Sciences / Clinical Research
Deliverable
client delivery
Required skills
ICH-GCP compliance, EU and FDA regulatory requirements, medical/therapeutic area knowledge, medical terminology, on-site monitoring execution
Preferred skills
Multi-national project team collaboration, independent work ownership
Technologies
Clinical trial management systems (implied by monitoring context)
Responsibilities
Perform and coordinate all aspects of the clinical monitoring process; conduct monitoring activities independently; deliver exemplary customer service on challenging projects
Seniority
Entry to Mid-level (6 months experience required)
