Manager, Program Coordinator.

작업 내용

Janssen Research & Development, LLC, a member of Johnson & Johnson’s Family of Companies, is recruiting for a Manager , Program Coordinator. This position can be located in Titusville, NJ; Raritan, NJ; Spring House, PA; Leiden, Netherlands; Beerse, Belgium; High Wycombe, United Kingdom; or Allschwil (Basel), Switzerland.

At the Janssen Pharmaceutical Companies of Johnson & Johnson, what matters most is helping people live full and healthy lives. We focus on treating, curing and preventing some of the most devastating and complex diseases of our time. And we pursue the most promising science, wherever it might be found.

Janssen Research & Development, LLC discovers and develops innovative medical solutions to address important unmet medical needs in oncology, immunology, neuroscience, infectious diseases and vaccines, cardiovascular and metabolism, and pulmonary hypertension. Please visit http://www.janssenrnd.com for more information.

The Manager, Program Coordinator (PC) will support the Project Management Leader (PML) in providing and maintaining cross-functional project plans utilizing systems and tools aligned across R&D. This individual will provide support to the Compound Development, Project Management, and Clinical Teams. Maintain integrated cross-functional project plans ensuring they are aligned with the compound development strategy. Create and communicate timeline, Full Time Equivalent (FTE), and Out-of-Pocket (OOP) reports to teams and management. The PC will create and review the project critical path analyses to ensure schedule risk is communicated and addressed by the teams. Provide cross-functional scenario planning and analyses to the teams. Facilitate team communications by maintaining and tracking cross-functional timelines, deliverables, and milestones including cross-project dependencies. The PC will be guided in all matters by our J&J Credo values and our Leadership Performance Standards.

Principal Responsibilities

• Maintain cross-functional project plans, team reports, and resource management support to ensure the completion of deliverables balanced for quality and timeliness.
• Assist the Program Management Leader (PML) in providing and maintaining system tools and cross-functional project plans aligned across R&D (Clinical, Pre-Clinical, Biomarker, Regulatory and Pharmaceutical development) to support the Compound Development Teams.
• Assist the PML in providing clinical cross-functional project plans aligned across the clinical functions (Clinical Pharmacology - small molecule only, Biostatistics, Programming, R&D Operations support, Regulatory, Quality Assistance and Quality Control) to support the Clinical Teams.
• As the program team resource manager, compile/generate program/project resource demands.
• Facilitate critical path analyses, contingency planning/scenario analyses, and propose strategies and solutions to modify schedules to keep the projects on track in collaboration with the PML.
• Generate program reports and communications to ensure team and program alignment of deliverable expectations.
• Provide overall support to the Clinical functional representatives to ensure completion of deliverables that are balanced for quality, timeliness, and resources.
• Facilitate project communications by maintaining and tracking timelines, deliverables, and milestones. Ensure project schedules, resources, and underlying assumptions are integrated and aligned across functions and provides coordination expertise.
• Assist the functions in determining scheduling and resource requirements.
• Conduct contingency planning and scenario analyses and proposes strategies and solutions to modify the schedules to keep projects on track.
• Provide regular reports and analysis on resource demand and supply.
• Facilitate regular review of workload and resource analyses, including business plans.
  
  

Qualifications

• A minimum of a Bachelor’s degree is required. Post-graduate degree preferred.
• A minimum of 5 years of related industry experience is required.
• A minimum of 3 years of experience in Drug Development is required.
• Knowledge of the end-to-end drug development process, including the ability to support all stages of drug development programs is required.
• Knowledge of clinical development/trial execution is required.
• Project management experience is required.
• Detailed knowledge of project planning, tracking, resource management, project planning, scheduling tools, and cross-project analyses is required.
• Professional Project Management certification and/or diploma is preferred.
• Experience with Planisware and/or Microsoft Project is preferred.
• Must have excellent communication, presentation and interpersonal skills.
• Must have strong leadership, decision-making and negotiating skills.
• The ability to lead project initiatives is required.
• The ability to collaborate will all levels of management and influence decision-making across a matrix environment is required.
• Travel to support project teams at multiple site locations will be required.
  
  

Johnson & Johnson is an Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability.

Primary Location

United States-New Jersey-Titusville-1125 Trenton Harbourton Road

Other Locations

Europe/Middle East/Africa-Belgium-Antwerp-Beerse, North America-United States-Pennsylvania-Spring House, North America-United States-New Jersey-Raritan, Europe/Middle East/Africa-United Kingdom-England-High Wycombe, Europe/Middle East/Africa-Netherlands-South Holland-Leiden, Europe/Middle East/Africa-Switzerland-Basel-City-Basel

Organization

Janssen Research & Development, LLC (6084)

Job Function

R&D

Requisition ID

2105980855W