Associate Director, Clinical PV & Medical Quality, CPMQ Global Regions

Company Name:

Takeda

Job Overview

The Associate Director, Clinical PV & Medical Quality, CPMQ Global Regions at Takeda provides oversight for regulated post-authorization activities from a clinical research and pharmacovigilance perspective.

Responsibilities

• Implementing global quality frameworks
• Ensuring compliance
• Managing investigations
• Supporting inspections

Key Requirements

• Scientific degree
• 10+ years of pharmaceutical experience (3+ in Quality/Compliance)
• Advanced knowledge of clinical research and medical affairs
• Strong communication and leadership skills