Associate Director PMO, Clinical Programs

Biopharma Careers; Irvine (CA); On-site; USD 137,000 - 236,000; Full time

Job summary

Johnson & Johnson is seeking an Associate Director PMO, Clinical Programs to drive enterprise integration across the clinical evidence portfolio. You will consolidate plans, align milestones with product development and regulatory priorities, and enable governance decisions through analytics and scenario planning.

The role owns the integrated portfolio roadmap, governance cadence, readiness management, and executive reporting, coordinating across Scientific Affairs, R&D, Regulatory, and Supply

Qualifications

• Bachelor’s degree in Life Sciences, Engineering, or related field is required.
• Advanced degree preferred (MS/MPH/MBA/PhD).
• 10+ years in clinical program or portfolio management within MedTech or life sciences.
• Familiar with PMO governance and portfolio management frameworks.
• Proficient in portfolio and project planning tools (Smartsheet, Power BI, Wrike, MS Project).

Responsibilities

• Own enterprise clinical portfolio integration and governance with cross-functional stakeholders.
• Consolidate function-owned study plans into an integrated portfolio view and enable governance decisions.
• Manage cross-functional RAID, readiness, and enterprise reporting for issuing escalations.
• Lead portfolio analytics, KPIs, and budget visibility to support prioritization decisions.

Skills

Portfolio management

Cross-functional collaboration

Communication skills

Data-driven decision making

Education

Bachelor’s degree in Life Sciences, Engineering, or related field

Advanced degree (MS, MPH, MBA, or PhD) preferred

PMP, PgMP, or MSP certification preferred

Lean Six Sigma or Agile certification a plus

Tools

Smartsheet

Power BI

Wrike

Microsoft Project

Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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 jnj.com

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Project/Program Management Group

Job Sub Function:

R&D Project Management

Job Category:

Professional

All Job Posting Locations:

Irvine, California, United States of America

Job Description:

The Associate Director PMO, Clinical Programs, is accountable for enterprise integration and decision enablement across the clinical evidence portfolio. The role consolidates function-owned clinical plans into an integrated portfolio view; connects clinical milestones with product development, regulatory, supply chain, finance, and commercial priorities; and enables governance decisions through portfolio analytics, scenario planning, prioritization, and cross-functional escalation.

This position owns the integrated portfolio roadmap, enterprise governance process, cross-functional dependency and readiness management, portfolio-level demand and capacity scenarios, consolidated reporting, and escalation of constraints that span multiple functions or programs. Scientific Affairs and Clinical Research retain ownership for clinical strategy, study design, operational plans, study schedules and deliverables, study-level risks and corrective actions, clinical budgets, CRO and vendor management, functional staffing, and leadership of Clinical Research Project Management personnel. The PMO role challenges, integrates, facilitates, recommends, and escalates; it does not direct study execution or create a parallel clinical delivery organization.

DUTIES & RESPONSIBILITIES

• Integrated Clinical Portfolio Roadmap: Own the enterprise clinical portfolio roadmap by consolidating approved, function-owned study plans and forecasts into a forward-looking view aligned with product development milestones, regulatory submissions, supply readiness, regional launches, lifecycle priorities, and post-market evidence commitments. Identify cross-program sequencing, dependencies, decision points, and readiness gaps; Clinical Research retains ownership of the underlying study plans, schedules, deliverables, and execution.
• Supply and Demand Integration: Translate approved study plans, enrollment forecasts, site activation schedules, and portfolio priorities into time-phased demand requirements for equipment, investigational products, components, and ancillary materials. Maintain a rolling forecast with Scientific Affairs, Supply Chain, Finance, and study teams; reconcile demand with inventory, capacity, lead times, shelf life, labeling, country requirements, and budget constraints.
• Governance and Executive Decision Support: Own the enterprise clinical portfolio governance cadence and decision package using validated inputs from accountable functional leaders. Frame portfolio-level choices, challenge assumptions, model cross-functional trade-offs, document decisions and decision rights, and track enterprise actions to closure. Clinical Research and other functional leaders retain authority for decisions within their functions and for study-level execution.
• Cross-Functional RAID and Readiness: Own the integrated view of risks, assumptions, issues, dependencies, constraints, and readiness gaps that affect multiple functions, programs, regulatory milestones, supply readiness, or launch commitments. Confirm functional ownership, facilitate coordinated resolution, and elevate unresolved portfolio-level constraints through governance. Clinical Research owns study-level risk identification, mitigation, corrective action, and operational resolution.
• Portfolio Analytics, KPIs, and Financial Visibility: Own consolidated portfolio reporting and analytics using approved milestones, KPIs, forecasts, assumptions, and budget inputs supplied by functional owners. Analyze schedule confidence, forecast accuracy, inventory exposure, capacity constraints, and portfolio trends to recommend prioritization and scenario decisions. Clinical Research and designated budget owners retain accountability for study budgets, forecasts, reconciliation, corrective action, and study-level performance reporting.
• Resource and Scenario Planning: Own portfolio-level demand, capacity, and scenario analyses using resource inputs supplied and approved by functional leaders. Recommend portfolio prioritization, sequencing, and mitigation options when demand exceeds capacity or enterprise milestones are at risk. Functional leaders retain decision authority for headcount, role assignments, performance management, and day-to-day deployment of their teams.
• Stakeholder Integration: Serve as the central PMO coordination point across Scientific Affairs, R&D, Regulatory, Quality, Supply Chain, Commercial, Finance, regional teams, and program leadership. Build alignment around portfolio assumptions, handoffs, milestones, evidence readiness, escalation pathways, and stakeholder expectations.
• PMO Maturity and Continuous Improvement: Own and continuously improve methods for enterprise clinical portfolio integration, demand forecasting, capacity planning, scenario analysis, governance, and executive reporting. Coach program and functional partners on integrated planning, escalation quality, decision framing, and portfolio reporting. Scientific Affairs retains ownership for Clinical Research operating procedures, technical project-management practices, and the development and performance management of Clinical Research Project Managers.

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 and project planning tools (Smartsheet, Power BI, Wrike, Microsoft Project, etc.)
• 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

Must be willing and able to periodically travel overnight domestically and internationally up to 25%.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers . Internal employees contact AskGS to be directed to your accommodation resource.

Preferred Skills

• Agility Jumps
• Business Alignment
• Collaboration
• Continuous Improvement
• Mentorship
• Operational Excellence
• Organizing
• Performance Measurement
• Process Control
• Project Management Methodology (PMM)
• Project Management Office (PMO)
• Project Reporting
• Project Schedule
• Quality Control (QC)
• Research and Development
• Technical Credibility

The anticipated base pay range for this position is :

$137,000.00 - $235,750.00

Additional Description for Pay Transparency

• Vacation –120 hours per calendar year
• Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year
• Holiday pay, including Floating Holidays –13 days per calendar year
• Work, Personal and Family Time - up to 40 hours per calendar year
• Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
• Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
• Caregiver Leave – 80 hours in a 52-week rolling period10 days
• Volunteer Leave – 32 hours per calendar year
• Military Spouse Time-Off – 80 hours per calendar year

For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits