Associate Director, Clinical Pv & Medical Quality, Cpmq Global Regions

Takeda

Massachusetts, United States
Base: $153,600.00 - $241,340.00; bonus/equity: not...
Clinical research expertise
Pharmacovigilance compliance
Global quality framework
The role provides oversight from a clinical research and pharmacovigilance perspective of regulated post-authorization activities

Job Summary

  • The role provides oversight from a clinical research and pharmacovigilance perspective of regulated post-authorization activities.
  • It drives a fit-for-use global Quality framework that elevates capabilities in business units.
  • The position requires collaboration with key stakeholders to support post-authorization strategies.

Matching Summary

The role provides oversight from a clinical research and pharmacovigilance perspective of regulated post-authorization activities.

Salary

Base: $153,600.00 - $241,340.00; Bonus/Equity: Not specified; Benefits: Medical, dental, vision insurance

Skills & Requirements

Must-have

  • Clinical research expertise
  • Pharmacovigilance compliance
  • Global Quality framework

Nice-to-have

  • Strong leadership skills
  • Excellent communication abilities
  • Proactive problem-solving

Key Requirements

  • BSc in scientific field
  • Minimum of 10 years experience
  • 3 years in Quality/Compliance

Work Rights

Not specified

Tailored Resume

Cover Letter