Regulatory Project And Resource Management Lead Ii

GlaxoSmithKline

Not specified
Project management experience in pharmaceutical industry
Experience with planisware or similar pm tools
Knowledge of regulatory development plans (rdp)
GlaxoSmithKline (GSK) is seeking a Regulatory Project and Resource Management Lead II to oversee regulatory support activities and ensure compliance in drug development. The ideal candidate will possess strong project management and analytical skills, fostering a culture of continuous improvement and collaboration within cross-functional teams

Job Summary

  • This role leads regulatory support activities to help bring science and technology to patients through optimized project delivery.
  • The position requires driving continuous improvement initiatives in project management, resource allocation, and risk management within a global R&D environment.
  • Candidates must possess strong project management principles and the ability to engage with stakeholders across multiple functional areas to ensure on-time delivery.

Matching Summary

Match Score: 85

GlaxoSmithKline (GSK) is seeking a Regulatory Project and Resource Management Lead II to oversee regulatory support activities and ensure compliance in drug development. The ideal candidate will possess strong project management and analytical skills, fostering a culture of continuous improvement and collaboration within cross-functional teams.

Skills & Requirements

Must-have

  • Project management experience in pharmaceutical industry
  • Experience with Planisware or similar PM tools
  • Knowledge of Regulatory Development Plans (RDP)
  • Ability to work in matrix environment
  • Drug development expectations and regulatory standards

Nice-to-have

  • PMP Certification (pursuing or completed)
  • Experience with Spotfire for data visualization
  • Strong analytical and problem-solving skills
  • Curiosity and drive to learn new technologies
  • Service-oriented attitude for interdisciplinary teams

Key Requirements

  • 7 years of experience in pharmaceutical business and drug development
  • Demonstrated experience with enterprise-wide project management tools
  • Sound knowledge of regulatory affairs from pre-IND through post-approval
  • Proven ability to manage integrated Regulatory Development Plans (RDPs)

Work Rights

Not specified

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