Senior Clinical Research Associate (Oncology Experience Required) - UK (Remote) - FSP - REGISTER YOUR INTEREST
Core
Senior Clinical Research Associate ensuring data integrity, compliance with ICH GCP, and protocol adherence at clinical trial sites.
Role type
Senior Clinical Research Associate (Oncology)
Builds
Clinical trial data and site compliance
Domain
Healthcare / Clinical Trials / Oncology
Deliverable
client delivery
Required skills
Oncology trial experience, RECIST criteria knowledge, ICH GCP compliance, data integrity management, source document review, protocol deviation management, informed consent verification, investigational product inventory management, remote monitoring execution
Preferred skills
Experience in CRO or Pharma trials environments
Technologies
Case Report Forms (CRF), Study Monitoring Plan (SMP), Clinical Monitoring Plan (CMP)
Responsibilities
Ensure regulatory and protocol compliance at site level; conduct source document review and verify clinical data accuracy; manage reporting and follow-up of protocol deviations; verify informed consent processes; manage investigational product inventory and administration; perform monitoring activities including remote and on-site visits.
Seniority
Senior, hands-on IC
