Principal Business Process Project Management Specialist - Clinical Pmo

Medtronic UK

Minneapolis, United States
Base: $129,600.00 - $194,400.00; bonus/equity: eli...
On-site
Manage clinical projects from initiation to completion
Develop and maintain detailed project plans
Track progress, identify risks, and ensure alignment
Medtronic is seeking a Principal Business Process Project Management Specialist to manage clinical projects within their Clinical Project Management Office. This role requires extensive project management expertise and a solid understanding of clinical research processes, with responsibilities encompassing project execution, operational management, risk management, and cross-functional leadership

Job Summary

  • As a Principal Business Process Project Management Specialist, you will support the Clinical Project Management Office (PMO) by managing and executing a portfolio of clinical projects, including post-market clinical studies and related initiatives.
  • Success in this role requires strong project management expertise combined with a solid understanding of clinical research processes, requirements, and cross-functional dependencies.
  • Medtronic offers a competitive Salary and flexible Benefits Package, including health, dental, vision insurance, 401(k) plan with employer contribution and match, and paid time off.

Matching Summary

Match Score: 85

Medtronic is seeking a Principal Business Process Project Management Specialist to manage clinical projects within their Clinical Project Management Office. This role requires extensive project management expertise and a solid understanding of clinical research processes, with responsibilities encompassing project execution, operational management, risk management, and cross-functional leadership.

Salary

Base: $129,600.00 - $194,400.00; Bonus/Equity: Eligible for MIP; Benefits: Health, Dental, Vision, 401(k), PTO, etc.

Skills & Requirements

Must-have

  • Manage clinical projects from initiation to completion
  • Develop and maintain detailed project plans
  • Track progress, identify risks, and ensure alignment
  • Oversee day-to-day operational aspects of projects
  • Maintain project dashboards and status reporting
  • Proactively identify project risks and issues
  • Lead and coordinate work across cross-functional teams

Nice-to-have

  • Experience in regulated or medical device environment
  • Familiarity with clinical study lifecycle
  • Proficiency with Smartsheet or similar tools
  • Experience with portfolio-level reporting
  • Ability to influence stakeholders without direct authority

Key Requirements

  • Bachelor's degree
  • 7+ years of experience in project management, clinical research, operations, or related field
  • Experience managing multiple complex, cross-functional projects in a matrixed environment
  • Experience supporting or working within clinical research

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter