Sr. Manager, Clinical Programs - PMO (Yokneam, Haifa District, Israel) Johnson and Johnson, MedTech Electrophysiology

This job is with Johnson & Johnson, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.

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:

Yokneam, Haifa District, Israel

Job Description

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

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 clinical evidence generation with market access, messaging, and customer needs.
  
  

Governance & Reporting

• Lead portfolio review meetings and contribute to PMO and executive steering governance.
• Maintain portfolio dashboards, KPIs, and risk registers for leadership visibility.
• Drive scenario planning and prioritization based on resource capacity, regulatory milestones, and market drivers.
• Ensure on-time readiness of clinical evidence for regulatory and commercial milestones.
• Ensure adherence to PMO governance standards, processes, and documentation practices.
  
  

Risk & Resource Management

• Identify and manage cross-program risks, resource optimization, constraints, and dependencies across the clinical and product lifecycle.
• Work closely with functional leaders to resolve resourcing or sequencing conflicts.
• Proactively escalate bottlenecks or misalignments that could impact evidence generation or launch readiness.
  
  

Continuous Improvement & PMO Maturity

• Contribute to the refinement of PMO methodologies for clinical portfolio management.
• Support implementation of best practices in forecasting, capacity planning, and performance reporting.
• Enable a culture of proactive portfolio management and data-driven decision-making.
  
  

Qualifications

• Bachelor's degree in Life Sciences, Engineering, or related field required.
• Advanced degree (MS, MPH, MBA, or PhD) preferred.
• 10+ years of experience in clinical program or portfolio management within MedTech, medical devices, diagnostics, or life sciences.
• Strong understanding of clinical study design, regulatory pathways, and product development processes.
• Demonstrated success managing cross-functional clinical portfolios tied to product launches or lifecycle management.
• Experience collaborating with R&D, Supply Chain, and Commercial functions on readiness and launch coordination.
• Familiarity with PMO governance and portfolio management frameworks.
• Proficient in portfolio planning tools (e.g., Smartsheet, Clarity, Planview, Power BI).
• Solid understanding of product development lifecycles and evidence requirements for market access.
• Strong analytical, prioritization, and resource management skills.
• Skilled communicator who can engage technical and business audiences with clarity and influence.
  
  

REQUIRED KNOWLEDGE, SKILLS, ABILITIES And CERTIFICATIONS/LICENSES

• PMP, PgMP, or MSP certification preferred.
• Lean Six Sigma or Agile certification a plus.
• Strategic integrator - Sees interconnections across programs and functions.
• Strong portfolio mindset - Prioritizes based on value, risk, and readiness.
• Influential communicator - Bridges clinical, technical, and commercial domains.
• Data-driven decision-maker - Leverages metrics and insights to guide trade-offs.
• Collaborative leader - Drives alignment and accountability across teams.
  
  

Additional Position Requirements

LOCATION & TRAVEL REQUIREMENTS

• Location: Irvine, CA or Haifa, Israel
• Travel: 25% expected travel for domestic, international, or both.
  
  

Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):

Additional posting, North America - R-041228

Required Skills

Preferred Skills:

Agile Decision Making, Analytics Insights, Developing Others, Inclusive Leadership, Leadership, Organizational Project Management, Performance Measurement, Program Management, Project Management Methodology (PMM), Project Management Office (PMO), Project Management Tools, Project Reporting, Regulatory Compliance, Risk Management, Statement of Work (SOW), Team Management