Sr. Principal Programming Portfolio Lead (associate Director)

Johnson & Johnson MedTech

Raritan, New Jersey, United States of America
Base: $137,000 - $235,750; bonus/equity: eligible ...
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Expert programming strategies and practices
Complex data structures and analysis
Project and people leadership skills
** Johnson & Johnson MedTech is seeking a Senior Principal Programming Portfolio Lead to oversee programming activities within its Innovative Medicine division. This role requires extensive experience in programming strategies and project leadership, focusing on clinical development and strategic innovation. **

Job Summary

  • The Senior Principal Portfolio Lead is responsible for formulating the Programming strategy across a large portfolio of one or more programs within a Disease area and/or Delivery Unit, with accountability for operational oversight and effective planning and execution of programming activities.
  • This position plays a critical role in the growth and development of C&SP (Clinical and Statistical Programming) and contributes to organizational effectiveness, transparency, and communication.
  • The role requires expert understanding of programming strategies, practices, methods, processes, technologies, industry standards, complex data structures, and analysis and reporting solutions.

Matching Summary

Match Score: 75

** Johnson & Johnson MedTech is seeking a Senior Principal Programming Portfolio Lead to oversee programming activities within its Innovative Medicine division. This role requires extensive experience in programming strategies and project leadership, focusing on clinical development and strategic innovation. **

Salary

Base: $137,000 - $235,750; Bonus/Equity: eligible for annual performance bonus; Benefits: medical, dental, vision, life insurance, disability, retirement plan, 401(k), paid time off

Skills & Requirements

Must-have

  • expert programming strategies and practices
  • complex data structures and analysis
  • project and people leadership skills
  • programming activities across teams
  • data analytics and reporting solutions
  • CDISC Standards knowledge

Nice-to-have

  • innovative thinking for programming strategies
  • business change and innovative ways of working
  • Oncology clinical trial experience

Key Requirements

  • 8+ years of experience in Pharmaceutical, CRO or Biotech industry
  • Bachelor's degree in Computer Sciences, Mathematics, Data Science/Engineering, Public Health, or related field
  • Expert knowledge of data structures and programming languages including Python
  • In-depth knowledge of programming practices, tools, and processes
  • In-depth knowledge of regulatory guidelines (e.g., ICH-GCP)
  • Project, risk, and team management experience
  • Experience managing outsourcing or externalization programming activities

Work Rights

Not specified

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