Associate Vice President, Quality

Amgen UK

Base: $266,028 - $359,920 usd annually; bonus/equi...
Not specified (assumed to be flexible based on the description).
Doctorate degree required
7+ years clinical & research quality experience
Ich e6r3 compliance expertise
Amgen UK is seeking an Associate Vice President of Quality to lead global quality strategies in clinical research across multiple therapeutic areas. The ideal candidate should possess extensive experience in clinical quality assurance and demonstrated leadership in managing teams and projects, particularly in compliance with regulatory standards. This role offers a competitive salary and comprehensive benefits, emphasizing professional growth and a collaborative work culture

Job Summary

  • This role leads the transformation of clinical quality oversight to ensure compliance with ICH E6R3 and embeds quality into development teams.
  • The successful candidate will drive inspection strategies globally and serve as the single point of accountability for R&D quality stakeholders.
  • Amgen offers a competitive salary range of $266,028 to $359,920 along with comprehensive benefits including retirement plans and stock incentives.

Matching Summary

Match Score: 85

Amgen UK is seeking an Associate Vice President of Quality to lead global quality strategies in clinical research across multiple therapeutic areas. The ideal candidate should possess extensive experience in clinical quality assurance and demonstrated leadership in managing teams and projects, particularly in compliance with regulatory standards. This role offers a competitive salary and comprehensive benefits, emphasizing professional growth and a collaborative work culture.

Salary

Base: $266,028 - $359,920 USD annually; Bonus/Equity: Discretionary annual bonus and stock-based long-term incentives; Benefits: Comprehensive health, dental, vision, retirement plan, and flexible work models

Skills & Requirements

Must-have

  • Doctorate degree required
  • 7+ years Clinical & Research Quality experience
  • ICH E6R3 compliance expertise
  • Risk-based quality management (RBQM)
  • Health authority inspection leadership

Nice-to-have

  • Experience with biosimilars and rare disease portfolios
  • Digital technology and data analytics capabilities
  • Collaborative inclusive leadership style
  • Proven track record in regulatory trends response

Key Requirements

  • Doctorate degree with 7 years experience OR Master's with 10 years OR Bachelor's with 12 years
  • 7 years of managerial experience leading multi-tiered organizations
  • Global oversight of large clinical trial programs across multiple therapeutic areas

Work Rights

Not specified

Tailored Resume

Cover Letter