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Associate Director, Accelerando Program Management (3 positions)

Associate Director, Accelerando Program Management (3 positions)

J&J Family of CompaniesWashington Crossing, PA, US
1 hour ago
Job type
  • Full-time
Job description

Associate Director, Accelerando Program Management

We are searching for the best talent for our Associate Director, Accelerando Program Management position to be located in Spring House, PA; Raritan, New Jersey or Titusville, New Jersey.

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Our Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures. We lead where medicine is going and need innovators with an unwavering commitment to results.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

The Associate Director, Accelerando Program Management combines project management expertise with advanced leadership capabilities, advising project teams to accelerate project execution and increase probability of success. Program Management Leaders are effective at maximising the network of internal expertise from across the J&J enterprise to facilitate success in our priority development programs.

You will be responsible for :

  • Partner with the highest priority new product development programs to de-risk and accelerate the launch of groundbreaking new products.
  • Proactively translate processes, knowledge, and expertise into specific solutions for individual teams during most impactful phases of the development program.
  • Apply exceptional facilitation and influencing skills to engage with development project team leaders, Therapy Area leaders, and functional partners across J&J to enable project success, and to act as a champion for the Accelerando team.
  • Support Compound Development Teams (CDT) by becoming a "trusted advisor" to project leadership and a strategic partner to functional team members. Assist CDT leadership in making informed and timely decisions by applying specific combination of proven experience, project management expertise, and leadership capabilities to facilitate program execution.
  • Applying expertise in project management tools and techniques, support the generation of project plans and provide insights based on customized project analysis and scenarios.
  • Bring clarity and focus to key project activities through critical path analysis based on fully integrated cross-functional project plan development; work with PMO partners to ensure alignment and integration with CDT project plan in Planisware.
  • Conduct objective Threats and Opportunity assessment of critical path to identify potential obstacles and enhance acceleration opportunities. Support early risk identification and development of mitigation strategies.
  • Drive the implementation of best practices to high value R&D development initiatives
  • Help ensure organizational readiness to support project execution.
  • Identify and communicate potential gaps in current cross-departmental processes and organizational structures, and work with line management to remove obstacles to effective project execution.
  • Proactively recommend and outline new processes for upcoming and current development phases. Help integrate enabling technologies into the team setting to drive clarity and efficiency.
  • Partner with project leadership to develop cases for the most impactful risk mitigation and acceleration opportunities.
  • Responsible for management and communication of metrics and benchmarking data on Accelerando process.
  • Actively monitor and engage externally to ensure a constant awareness of emerging new practices, project management and leadership tools and strategies, and continuous improvement opportunities for Accelerando.

Qualifications / Requirements :

  • A minimum of a Bachelor's degree is required
  • A minimum of 7 years of relevant experience in an R&D or Supply Chain environment
  • Professional project management certification (i.e., PMP, CPM, etc.) is preferred
  • Critical Chain Experience / Pro-Chain Certification is a plus
  • Demonstrated expertise in MS Project is required
  • Proficiency with technology enabling tools including Visio, Excel required
  • Proven ability to be creative and flexible to change / improve working environment in broad context is required
  • Experience working in a global matrixed organization is required
  • Candidate must be able to work in one of the following locations : Raritan, NJ, Spring House, PA, Titusville, NJ, High Wycombe, UK or Beerse, BE.
  • Other :

  • May require up to 20% travel for brief durations dependent on project assignment.
  • 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.

    Required 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

    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-$235,750

    The expected base pay range for this position is $137,000-$235,750. The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market. The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation's performance over a calendar / performance year. Bonuses are awarded at the Company's discretion on an individual basis. Subject to the terms of their respective plans, employees and / or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs : medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance. 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)). 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 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 Condolence Leave 30 days for an immediate family member : 5 days for an extended family member Caregiver Leave 10 days Volunteer Leave 4 days Military Spouse Time-Off 80 hours Additional information can be found through the link below. For additional general information on Company benefits, please go to : https : / / www.careers.jnj.com / employee-benefits This job posting is anticipated to close on December 3, 2025. The Company may however extend this time-period, in which case the posting will remain available on https : / / www.careers.jnj.com to accept additional applications.

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