Clinical Research Associate (cra) – Oncology Studies (6+ Months) - Sponsor Dedicated - Türkiye

IQVIA UK

Türkiye
On-site
Oncology studies experience
Site monitoring activities
Gcp and ich guidelines
IQVIA Türkiye is seeking an experienced Clinical Research Associate (CRA) specializing in oncology studies for a minimum six-month contract. The role involves site management, monitoring clinical trials, ensuring compliance with regulations, and supporting study progress

Job Summary

  • Perform monitoring and site management activities to ensure that clinical trial sites conduct studies and report data in accordance with the study protocol, applicable regulations, and sponsor requirements.
  • Conduct site monitoring visits including site selection, initiation, routine monitoring, and close‑out visits in line with contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines.
  • Ensure essential documents are complete and properly filed within the Trial Master File (TMF) and verify that the Investigator Site File (ISF) is maintained in compliance with GCP, ICH, and local regulatory requirements.

Matching Summary

Match Score: 85

IQVIA Türkiye is seeking an experienced Clinical Research Associate (CRA) specializing in oncology studies for a minimum six-month contract. The role involves site management, monitoring clinical trials, ensuring compliance with regulations, and supporting study progress.

Skills & Requirements

Must-have

  • Oncology studies experience
  • Site monitoring activities
  • GCP and ICH guidelines
  • Trial Master File (TMF)
  • Investigator Site File (ISF)

Nice-to-have

  • Adapt and drive subject recruitment
  • Cross-functional study team collaboration
  • Effective working relationships

Key Requirements

  • Minimum 6 months of on-site monitoring experience in oncology clinical studies
  • Previous CRA experience
  • Bachelor’s degree in a scientific discipline or healthcare field preferred

Work Rights

Not specified

Tailored Resume

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