Phase 1 Oncology Monitoring Specialist

3 weeks ago


Toulouges, Occitanie, United States IQVIA Full time
About IQVIA

IQVIA is committed to providing equal employment opportunities for all, including veterans and candidates with disabilities.

Career Overview

This role offers an exciting opportunity for a motivated and detail-oriented individual to join our team as a Clinical Research Associate. You will be responsible for monitoring and managing clinical trial sites to ensure compliance with study protocols, regulations, and sponsor requirements.

Job Responsibilities
  • Conduct site monitoring visits to ensure adherence to GCP and ICH guidelines
  • Collaborate with sites to develop and track recruitment plans
  • Provide protocol and study training to sites
  • Assess site practices for protocol adherence and regulatory compliance
Salary Range

The potential base pay range for this role is $71,900.00 - $189,000.00 per year, depending on qualifications and experience.



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