[innovative Medicine] R&d, Senior Programing Lead, Clinical & Statistical Programming Japan

Johnson & Johnson Innovative Medicine

Chiyoda, Japan
Not specified
Sas programming expertise
Post-marketing surveillance programming
Vendor management oversight
Johnson & Johnson Innovative Medicine is seeking a Senior Programming Lead for Clinical & Statistical Programming in Chiyoda, Japan, to oversee programming activities related to post-marketing surveillance studies. The ideal candidate will have extensive programming experience, particularly in handling complex datasets and regulatory compliance, and will play a key role in ensuring high-quality outputs in collaboration with various stakeholders

Job Summary

  • The Senior Programming Lead drives the standardization of PMS programming processes and delivers high-quality outputs in partnership with multiple internal and external stakeholders.
  • This role plans and manages end-to-end PMS programming projects, coordinating resources and ensuring adherence to applicable regulations and internal SOPs.
  • Johnson & Johnson is committed to healthcare innovation that empowers the prevention, treatment, and cure of complex diseases with smarter and less invasive solutions.

Matching Summary

Match Score: 85

Johnson & Johnson Innovative Medicine is seeking a Senior Programming Lead for Clinical & Statistical Programming in Chiyoda, Japan, to oversee programming activities related to post-marketing surveillance studies. The ideal candidate will have extensive programming experience, particularly in handling complex datasets and regulatory compliance, and will play a key role in ensuring high-quality outputs in collaboration with various stakeholders.

Skills & Requirements

Must-have

  • SAS programming expertise
  • Post-marketing surveillance programming
  • Vendor management oversight
  • Cross-functional team collaboration
  • Programming process standardization
  • Project and team management skills

Nice-to-have

  • Knowledge of ICH-GCP guidelines
  • Expertise in CDISC standards
  • Strong written and verbal English communication
  • Experience with clinical R&D concepts
  • Data manipulation and statistical analysis

Key Requirements

  • Bachelor’s degree or higher in relevant scientific field
  • 4+ years programming experience preferably in PMS environment
  • Knowledge of applicable PMS regulations
  • Demonstrated experience leading programming teams
  • Experience with standardized dataset and data presentation templates
  • Working knowledge of post-marketing regulatory requirements

Work Rights

Not specified

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