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CRA 2, Oncology, IQVIA

IQVIA · Durham, NC +3 more

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Clinical OperationsFull-time$90k–$150kCompany career page

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Role summary

IQVIA seeks a Clinical Research Associate 2 for oncology studies with 1.5+ years of on-site monitoring experience. The role involves conducting site monitoring visits, managing recruitment, ensuring protocol compliance, and maintaining regulatory documentation across multiple locations.

What they're looking for

  • Bachelor's degree, preferably in scientific or healthcare discipline
  • 1.5 to 2 years of CRA experience including on-site monitoring
  • Knowledge of Good Clinical Practice (GCP) and ICH guidelines
  • Experience with protocol training and site management
  • Proficiency in clinical trial documentation and regulatory requirements
  • Oncology study experience

What you'll be doing

  • Conduct site selection, initiation, monitoring, and close-out visits per protocol and regulatory standards
  • Partner with sites to develop and track subject recruitment plans
  • Administer protocol training and establish ongoing communication with study sites
  • Review site practices for protocol adherence and regulatory compliance; escalate quality issues
  • Track study progress including approvals, enrollment, CRF completion, and data queries

Key requirements

Therapeutic area
Oncology

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