Associé(e) De Recherche Clinique (arc) Principal(e) / Senior Clinical Research Associate, Sponsor Dedicated

IQVIA

Montreal, Canada
Base: $102,500.00 - $152,500.00; bonus/equity: not...
Site monitoring visits
Subject recruitment planning
Protocol and study training
Perform site monitoring visits including selection, initiation, monitoring, and close-out in accordance with contracted scope of work and regulatory requirements

Job Summary

  • Perform site monitoring visits including selection, initiation, monitoring, and close-out in accordance with contracted scope of work and regulatory requirements.
  • Administer protocol and study training to assigned sites, establish regular communication, and manage ongoing project expectations and issues.
  • Act as a mentor for clinical staff, collaborate with study team members, and ensure site documentation is maintained according to GCP/ICH guidelines.

Matching Summary

Perform site monitoring visits including selection, initiation, monitoring, and close-out in accordance with contracted scope of work and regulatory requirements.

Salary

Base: $102,500.00 - $152,500.00; Bonus/Equity: Not specified; Benefits: Health and wellness benefits offered

Skills & Requirements

Must-have

  • Site monitoring visits
  • Subject recruitment planning
  • Protocol and study training
  • GCP and ICH guidelines
  • Data query generation and resolution

Nice-to-have

  • Mentoring clinical staff
  • Effective time management
  • Building client relationships
  • Financial management of sites

Key Requirements

  • Minimum 3 years on-site monitoring experience
  • Bachelor's Degree in science or healthcare preferred
  • Proficiency in Microsoft Office Suite
  • Bilingual French and English required

Work Rights

Not specified

Tailored Resume

Cover Letter