Sr. Cra 1, Oncology, Iqvia Biotech

IQVIA Biotech

Base: $87,200.00 - $169,300.00 annually; bonus/equ...
Not specified
2 years on-site monitoring experience
Oncology therapeutic area expertise
Good clinical practice (gcp) knowledge
IQVIA Biotech is seeking a Senior Clinical Research Associate (CRA) with at least 2 years of oncology monitoring experience to manage site activities and ensure compliance with study protocols. The role involves performing monitoring visits, managing site communications, and ensuring data integrity throughout the clinical trial process

Job Summary

  • IQVIA Biotech is a full-service CRO with over 25 years of experience serving biotech sponsors to bring breakthrough treatments to patients faster.
  • The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with Good Clinical Practice.
  • Candidates must ensure study data reporting aligns with the protocol, applicable regulations, and sponsor requirements while managing subject recruitment plans.

Matching Summary

Match Score: 85

IQVIA Biotech is seeking a Senior Clinical Research Associate (CRA) with at least 2 years of oncology monitoring experience to manage site activities and ensure compliance with study protocols. The role involves performing monitoring visits, managing site communications, and ensuring data integrity throughout the clinical trial process.

Salary

Base: $87,200.00 - $169,300.00 annually; Bonus/Equity: Dependent on position; Benefits: Health, welfare, and other benefits offered

Skills & Requirements

Must-have

  • 2 years on-site monitoring experience
  • Oncology therapeutic area expertise
  • Good Clinical Practice (GCP) knowledge

Nice-to-have

  • Agile project execution approach
  • Strong site relationship management
  • Data integrity evaluation skills

Key Requirements

  • Bachelor's Degree in scientific discipline or health care preferred
  • Minimum 2 years of on-site monitoring experience
  • Knowledge of ICH guidelines and local regulatory requirements

Work Rights

Not specified

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