Assoc Dir, Clinical Pharmacovigilance And Medical Quality (cpmq) Operations (hybrid)

Takeda UK

Boston, MA, United States
Base: $154,400.00 - $242,550.00; bonus/equity: not...
On-site
Strategic quality leadership
Regulatory alignment
Operational excellence
Advance strategic quality leadership by embedding global standards across Clinical, Pharmacovigilance, and Medical Quality (CPMQ), ensuring regulatory alignment and operational excellence

Job Summary

  • Advance strategic quality leadership by embedding global standards across Clinical, Pharmacovigilance, and Medical Quality (CPMQ), ensuring regulatory alignment and operational excellence.
  • Drive innovation and transformation through organizational planning, digitalization, and capability building—enhancing systems, analytics, and process efficiency across CPMQ and R&D.
  • Strengthen quality oversight and risk management, leading compliance strategies, monitoring systems, and continuous improvement initiatives that mitigate systemic risks and foster resilience.

Matching Summary

Advance strategic quality leadership by embedding global standards across Clinical, Pharmacovigilance, and Medical Quality (CPMQ), ensuring regulatory alignment and operational excellence.

Salary

Base: $154,400.00 - $242,550.00; Bonus/Equity: Not specified; Benefits: Medical, dental, vision insurance, 401(k) plan and company match, disability coverage, life insurance, tuition reimbursement, paid volunteer time off, company holidays, well-being benefits, sick time, paid vacation

Skills & Requirements

Must-have

  • strategic quality leadership
  • regulatory alignment
  • operational excellence
  • organizational planning
  • digitalization
  • capability building
  • quality oversight
  • risk management
  • compliance strategies
  • continuous improvement initiatives

Nice-to-have

  • adaptive thinking
  • critical mindset
  • forward-thinking
  • adaptable to dynamic situations
  • culture of learning

Key Requirements

  • BSc/BA degree
  • Minimum of 5 years of relevant experience
  • Experience in pharmaceutical R&D, project management, strategy, or innovation in a regulated environment

Work Rights

Not specified

Tailored Resume

Cover Letter