Sr. Manager, Clinical Programs - PMO (Irvine, CA) Johnson and Johnson, MedTech Electrophysiology

At Johnson & Johnson, we believe health is everything.

Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

Job Function:
Project/Program Management Group

Job Sub Function:
Project/Program Management

Job Category:
People Leader

All Job Posting Locations:
Irvine, California, United States of America

Job Description:

JOB SUMMARY

Johnson & Johnson MedTech Electrophysiology is recruiting for a Clinical Research, Manager, to support the Electrophysiology (EP) business unit based in Irvine, CA.

The Senior Clinical Program Manager (CPM) within the PMO leads the strategic coordination, prioritization, and portfolio management of all clinical programs.

This role ensures clinical activities are aligned with product development, regulatory strategy, and commercial launch timelines, while maintaining visibility and accountability across the full clinical evidence portfolio.

Acting as a central integrator between Scientific Affairs, R&D, Regulatory, Supply Chain, and Commercial, the CPM drives governance, reporting, and readiness across interdependent programs to enable informed decision-making and optimized resource allocation.

 

DUTIES & RESPONSIBILITIES

Under (e.g.

limited supervision, general direction, etc.) and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position manages the following responsibilities:

 

Portfolio & Program Oversight


* Lead portfolio-level planning, prioritization, and tracking of all clinical studies supporting new product development, lifecycle management, and post-market evidence.


* Manage the clinical roadmap in alignment with R&D development milestones, regulatory submissions, and commercial launch timelines.


* Ensure visibility of interdependencies across programs, including clinical, technical, and operational linkages.


* Partner with Scientific Affairs to maintain a consolidated, forward-looking portfolio view of study status, timelines, and budget allocations.

Cross-Functional Alignment


* Serve as the central point of coordination between Scientific Affairs, R&D, Regulatory, Supply Chain, and Commercial teams, driving alignment and stakeholder satisfaction.


* Ensure clinical program plans align with product development schedules and launch strategies.


* Collaborate with Supply Chain to ensure clinical and launch readiness, including product availability, labeling, and logistics for study or launch execution.


* Partner with Commercial teams to align cl...