Clinical Research Associate 2 - Based In Portugal

IQVIA

Lisbon, Portugal
Site selection and monitoring
Subject recruitment planning
Regulatory compliance
Performing site selection, initiation, monitoring and close-out visits, and evaluating site practices in accordance with regulatory requirements

Job Summary

  • Performing site selection, initiation, monitoring and close-out visits, and evaluating site practices in accordance with regulatory requirements.
  • Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions.
  • IQVIA offers resources for career growth, supportive leaders, and programs to build therapeutic knowledge within an excellent working environment.

Matching Summary

Performing site selection, initiation, monitoring and close-out visits, and evaluating site practices in accordance with regulatory requirements.

Skills & Requirements

Must-have

  • site selection and monitoring
  • subject recruitment planning
  • regulatory compliance
  • data query resolution
  • client collaboration

Nice-to-have

  • career growth resources
  • flexible work schedules
  • therapeutic knowledge building
  • diversity and inclusion

Key Requirements

  • University degree in scientific discipline
  • 2-4 years independent on-site monitoring
  • Very good computer skills
  • Excellent command of Portuguese and English
  • Flexibility to travel
  • Driver’s license class B

Work Rights

Not specified

Tailored Resume

Cover Letter