Manager, Project Management Clinical Ep

Johnson & Johnson MedTech

Irvine, California, United States of America
Base: $117,000.00 - $201,250.00; bonus/equity: not...
Hybrid (3 days onsite, 2 days remote)
Clinical trial management
Cross-functional team leadership
Risk management and mitigation
Johnson & Johnson MedTech is seeking a Clinical Research Project Manager for their Electrophysiology business in Irvine, California. The ideal candidate will have extensive experience in clinical research leadership and project management, with a strong focus on cross-functional collaboration and operational excellence

Job Summary

  • The Clinical Research Project Manager will be responsible for clinical trial management within the Clinical R&D Department while fostering strong, productive relationships with colleagues across the organization.
  • Provide day‑to‑day leadership to project team members, fostering strong planning, risk management, and disciplined execution while mentoring the project management team on best practices.
  • The anticipated base pay range for this position is : $117,000.00 - $201,250.00.

Matching Summary

Match Score: 85

Johnson & Johnson MedTech is seeking a Clinical Research Project Manager for their Electrophysiology business in Irvine, California. The ideal candidate will have extensive experience in clinical research leadership and project management, with a strong focus on cross-functional collaboration and operational excellence.

Salary

Base: $117,000.00 - $201,250.00; Bonus/Equity: Not specified; Benefits: Vacation –120 hours per calendar year, Sick time - 40-56 hours per calendar year, Holiday pay –13 days per calendar year, Work, Personal and Family Time - up to 40 hours per calendar year, Parental Leave – 480 hours, Bereavement Leave – 240 hours/40 hours, Caregiver Leave – 80 hours, Volunteer Leave – 32 hours, Military Spouse Time-Off – 80 hours

Skills & Requirements

Must-have

  • Clinical trial management
  • Cross-functional team leadership
  • Risk management and mitigation
  • Project timeline integration
  • Regulatory compliance (ICH-GCP, ISO 14155)

Nice-to-have

  • Mentoring project teams
  • Process optimization
  • Vendor collaboration
  • Strategic decision support

Key Requirements

  • Bachelor's Degree in Life Science or related
  • 8+ years scientific/technical experience
  • Leadership/management role in Clinical Research
  • Significant clinical project leadership experience
  • Experience building consensus with cross-functional teams
  • Clinical/medical background required
  • 1-2 years people management experience preferred

Work Rights

Not specified

Tailored Resume

Cover Letter