CRA I/II - FSP - UK - Vaccines
Core
Conduct independent on-site clinical monitoring for vaccine and oncology studies to ensure data quality and regulatory compliance.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory adherence for pharmaceutical clients
Domain
Life Sciences / Clinical Research / Vaccines
Deliverable
client delivery
Required skills
ICH-GCP knowledge, EU and FDA regulatory requirements, medical/therapeutic area knowledge, medical terminology, independent on-site monitoring
Preferred skills
Experience in Vaccine or Oncology studies
Technologies
None stated
Responsibilities
Perform and coordinate all aspects of the clinical monitoring process; conduct monitoring activities independently; thrive in multi-national project teams
Seniority
Entry-level to Mid-level (1+ years experience)
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