Clinical Research Associate Oncology Trials Coordinator

2 weeks ago


Toulouges, Occitanie, United States IQVIA Full time
About IQVIA

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

Career Overview

We are seeking a highly skilled Clinical Research Associate (CRA) to join our dynamic team as a Clinical Research Associate You'll play a pivotal role in monitoring and managing clinical trial sites to ensure compliance with study protocols, regulations, and sponsor requirements. Be at the forefront of groundbreaking cancer research and make a real impact on patients' lives.

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
  • Oversee regulatory submissions, recruitment, enrollment, CRF completion, and data query resolution
  • Ensure all site documents are filed in the Trial Master File (TMF) and Investigator's Site File (ISF)
Requirements
  • Bachelor's degree in a scientific discipline or healthcare preferred
  • 3+ years of on-site oncology monitoring experience strongly preferred
  • Phase 1 oncology experience required
  • Proficient in GCP and ICH guidelines
  • Strong therapeutic and protocol knowledge in Phase 1 oncology trials
Benefits

We offer a competitive salary range of $71,900 - $189,000 per year, depending on qualifications and experience. Additionally, we provide a range of health and welfare benefits.



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