Regulatory And Start Up Manager (com)

IQVIA UK

Amsterdam, Netherlands
Hybrid
Dutch language fluency
Experience in international roles
Knowledge of drug development process
The role involves managing site activation and regulatory activities for clinical studies

Job Summary

  • The role involves managing site activation and regulatory activities for clinical studies.
  • Collaboration across regions is essential to ensure compliance and project delivery.
  • The position requires a thorough understanding of clinical trial regulations and processes.

Matching Summary

The role involves managing site activation and regulatory activities for clinical studies.

Skills & Requirements

Must-have

  • Dutch language fluency
  • Experience in international roles
  • Knowledge of drug development process

Nice-to-have

  • Leadership and mentoring skills
  • Strong regulatory writing skills

Key Requirements

  • Bachelor's Degree in Life sciences
  • 7 years relevant experience
  • Knowledge of GCP and ICH guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter