Statistical Programming Lead

Johnson & Johnson

Raritan, New Jersey, United States of America
Base: $109,000.00 - $174,800.00; bonus/equity: ann...
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Statistical programming with sas and r
Clinical trial data analysis and reporting
Cross-functional team collaboration
** Johnson & Johnson is seeking a Statistical Programming Lead to oversee programming activities for clinical trials, ensuring compliance with industry standards and quality deliverables. The ideal candidate will have a strong background in programming, project management, and collaboration across functional teams, with expertise in tools such as SAS and R. **

Job Summary

  • The Statistical Programming Lead is responsible for providing expertise, planning and oversight of programming trial activities of moderate to high complexity, ensuring high-quality and timely deliverables.
  • Johnson & Johnson offers a competitive compensation package including base salary, annual performance bonus, and comprehensive employee benefits such as medical, dental, vision, retirement plans, and various leave options.
  • The role involves collaboration with internal and external stakeholders, contributing to departmental innovation, and supporting clinical programs from lab to life while championing patients every step of the way.

Matching Summary

Match Score: 75

** Johnson & Johnson is seeking a Statistical Programming Lead to oversee programming activities for clinical trials, ensuring compliance with industry standards and quality deliverables. The ideal candidate will have a strong background in programming, project management, and collaboration across functional teams, with expertise in tools such as SAS and R. **

Salary

Base: $109,000.00 - $174,800.00; Bonus/Equity: Annual performance bonus discretionary; Benefits: Medical, dental, vision, life insurance, disability, retirement plans, paid time off

Skills & Requirements

Must-have

  • Statistical programming with SAS and R
  • Clinical trial data analysis and reporting
  • Cross-functional team collaboration
  • Regulatory compliance and GCP knowledge
  • Programming strategy and oversight
  • CDISC standards implementation

Nice-to-have

  • Python programming skills
  • Vendor management oversight experience
  • Process improvement and innovation
  • Project management skills
  • Data visualization and reporting

Key Requirements

  • Bachelor’s degree or higher in relevant field
  • 4+ years programming or clinical data management experience
  • Knowledge of ICH-GCP and clinical R&D concepts
  • Experience leading programming teams
  • Expertise in CDISC standards preferred

Work Rights

Not specified

Tailored Resume

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