Regulatory And Start Up Specialist

IQVIA UK

Paris, France
Hybrid
Fluency in french
Knowledge of gcp/ich guidelines
Experience in clinical research
The role involves serving as the Single Point of Contact for investigative sites and project teams

Job Summary

  • The role involves serving as the Single Point of Contact for investigative sites and project teams.
  • Responsibilities include ensuring adherence to SOPs and project timelines.
  • The position requires preparation and review of regulatory documents for clinical trials.

Matching Summary

The role involves serving as the Single Point of Contact for investigative sites and project teams.

Skills & Requirements

Must-have

  • Fluency in French
  • Knowledge of GCP/ICH guidelines
  • Experience in clinical research

Nice-to-have

  • Good negotiating and communication skills
  • Ability to challenge decisions
  • Local expertise in project planning

Key Requirements

  • Bachelor’s Degree in life sciences
  • 3 years’ clinical research experience

Work Rights

Not specified

Tailored Resume

Cover Letter