Johnson & Johnson

Sr Manager Accelerando Program Lead

Johnson & Johnson$137K — $235K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Life Sciences, Nursing, Pharmacy, Business, or related discipline required.
  • 8+ years experience in pharmaceutical, healthcare, biotechnology, or related industries.
  • Experience leading complex clinical development programs.
  • Familiarity with project management methodologies, systems, and tools.
  • Expertise in MS Project and proficiency in supporting tech tools like Visio and Excel.
  • Strong leadership, communication, and analytical skills.
  • Experience in matrix organizations and mentoring/coaching others.

Responsibilities

  • Create and manage integrated study schedules in Microsoft Project.
  • Identify opportunities to shorten development timelines while ensuring quality.
  • Leverage digital tools and analytics for improved program execution.
  • Align clinical trial timelines with broader development strategies.
  • Proactively manage risks and dependencies throughout projects.
  • Facilitate alignment among cross-functional stakeholders to address challenges.
  • Drive the adoption of project management best practices and improvements.

Benefits

  • 401(k) and pension plan participation eligible.
  • 120 hours of vacation per year.
  • Up to 40 hours of personal and family time annually.
  • 480 hours of parental leave for new parents.
  • Various forms of leave including caregiver and volunteer time.
  • Support for military spouses with designated time off.
Full Job Description
Job Function:
R&D Operations

Job Sub Function:
Clinical Trial Project Management

Job Category:
Professional

All Job Posting Locations:
Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America

Job Description:

Johnson & Johnson is currently seeking a Senior Manager, Accelerando Program Leader to join our team located in either of these locations Beerse, Belgium, Spring House PA, Raritan/Titusville NJ, United States. Office presence is required 3 times a week.

The Senior Manager, Accelerando Program Leader is accountable for accelerating the delivery of complex clinical development programs through integrated planning, proactive risk management, cross functional orchestration, and strategic decision support.

The Accelerando Program Leader identifies and protects the critical path, reduces uncertainty early, drives enterprise-level decision making, and ensures alignment between development strategy and operational execution.

The Accelerando Program Management Leader combines project management expertise with advanced leadership capabilities, consulting with project teams to accelerate project execution and increase probability of success.

Primary responsibilities:

Create, maintain, and manage integrated study schedules in Microsoft Project including key events, roadmaps, and critical-path visualizations.

Identify opportunities to accelerate development timelines while maintaining quality and compliance.

Leverage digital planning platforms, integrated timelines, predictive analytics, dashboards, and program management tools to improve predictability and execution.

Align clinical trial timelines with integrated clinical and compound development plans.

Identify and proactively manage risks, issues, assumptions, decisions, and dependencies.

Maintain study governance documentation, After Action Review and lessons learned.

Support governance reviews, investment decisions, and portfolio prioritization activities.

Partner with project and compound development leadership as a trusted advisor to accelerate delivery of high-priority development programs and support strategic decision making.

Facilitate alignment among project leaders, therapeutic area leadership, and cross-functional stakeholders to address barriers, drive accountability, and enable successful program execution.

Conduct critical path analyses and objective threat-and-opportunity assessments to identify acceleration opportunities, remove obstacles, reduce execution risk, and improve development predictability.

Develop and evaluate strategic scenarios and business cases supporting risk mitigation investments, acceleration opportunities, and key development decisions.

Drive implementation and adoption of project management best practices, innovative methodologies, and enabling technologies that improve development effectiveness and efficiency.

Identify process, organizational, and cross-functional execution gaps and partner with stakeholders and line management to implement sustainable improvements that enhance program delivery.

Support organizational readiness and change-management activities required to execute development strategies effectively across global teams.

Establish, monitor, and communicate program performance metrics, benchmarking insights, lessons learned, and continuous improvement opportunities to project leadership and governance bodies.

Build and leverage internal and external networks to identify emerging industry practices, benchmark performance, and promote knowledge sharing across development teams and strategic partners.

Monitor advancements in project management, leadership practices, digital technologies, and development strategies, integrating relevant innovations to strengthen Accelerando capabilities and accelerate delivery.

Champion the Accelerando approach and contribute to the evolution of program acceleration capabilities across the development organization.

Qualifications / Requirements:

Minimum of a Bachelor's degree in Life Sciences, Nursing, Pharmacy, Business, or related discipline is required.

Minimum 8 years of experience in pharmaceutical, healthcare, biotechnology, or related industries.

Demonstrated experience leading complex clinical development programs.

Knowledge of project management methodologies, systems, and tools.

Demonstrated expertise in MS Project.

Proficiency with technology enabling tools including Visio, Excel, etc.

Excellent leadership, communication, presentation, analytical, and decision-making skills.

Experience mentoring/coaching others.

Experience operating in matrixed global organizations and leading without authority.

Demonstrated ability to be creative and flexible to change/improve working environment in broad context.

Preferred:

Professional project management certification (i.e., PMP, CPM, etc.)

Hands on experience in Planisware

Required Skills:

Preferred Skills:
Budgeting, Clinical Trial Designs, Clinical Trials, Compliance Management, Consulting, Contract Management, Execution Focus, Fact-Based Decision Making, Give Feedback, Industry Analysis, Laboratory Operations, Organizing, Process Improvements, Project Integration Management, Research and Development, Research Ethics, Technical Credibility

The anticipated base pay range for this position is :
$137,000.00 - $235,750.00

Additional Description for Pay Transparency:
Subject to the terms of their respective plans, employees are eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).

This position is eligible to participate in the Company's long-term incentive program.

Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:

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

About Johnson & Johnson

Scio Diamond creates single-crystal Type IIa diamonds for the jewelry market and for industrial applications. It employs a patent-protected chemical vapor deposition (CVD) process in a precisely controlled laboratory setting to produce diamonds. It was founded in 2009 and is headquartered in Greenville, South Carolina.

Johnson & Johnson Careers

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Learn more about Johnson & Johnson
Size
141,700 employees
Market Cap
$462.7 billion
Industry
Net Income
$14.7 billion
Founded
1886
5 Year Trend
+5.5%
Revenue
$82.5 billion
NASDAQ

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