Associate Director Regulatory Affairs

IQVIA Inc

8 years relevant experience
6 years regulatory experience
Extensive regulatory writing skills
The role involves acting as a Project Manager for large stand-alone programmes involving multiple regulatory deliverables and regions

Job Summary

  • The role involves acting as a Project Manager for large stand-alone programmes involving multiple regulatory deliverables and regions.
  • Candidates must provide strategic regulatory consultancy and manage meetings with Regulatory Agencies while defending costs and timelines to clients.
  • The position requires extensive experience in regulatory writing and the ability to exercise independent judgement when making calculated risks.

Matching Summary

The role involves acting as a Project Manager for large stand-alone programmes involving multiple regulatory deliverables and regions.

Skills & Requirements

Must-have

  • 8 years relevant experience
  • 6 years regulatory experience
  • extensive regulatory writing skills
  • advanced negotiating skills
  • independent judgement capability

Nice-to-have

  • mentorship to junior colleagues
  • positive attitude under pressure
  • innovative solution delivery
  • diplomatic interaction style
  • workshop presentation skills

Key Requirements

  • Bachelor's or Master's Degree in Lifescience
  • At least 8 years total relevant experience
  • Minimum 6 years specific regulatory experience
  • Applicable certifications and licenses by country/state

Work Rights

Not specified

Tailored Resume

Cover Letter