Head Of China Statistics

Pfizer

Shanghai, China
On-site
Biometrics vision and strategy for r&d
Innovative trial designs
Ai applications in biostatistics
Pfizer is seeking a Head of China Statistics to lead the biometrics vision and strategy for R&D in China, ensuring alignment with global objectives. The role requires extensive experience in clinical development and project management, with a focus on innovative trial designs and regulatory compliance

Job Summary

  • Set and drive the biometrics vision and strategy for R&D within China across early and late development, ensuring alignment with overall global R&D objectives.
  • Partner effectively with global and China Clinical Development, Regulatory Affairs, Safety, Clinical Pharmacology and Real World Evidence, and other functions.
  • Develop people, including recruitment, retention, and career development.

Matching Summary

Match Score: 85

Pfizer is seeking a Head of China Statistics to lead the biometrics vision and strategy for R&D in China, ensuring alignment with global objectives. The role requires extensive experience in clinical development and project management, with a focus on innovative trial designs and regulatory compliance.

Skills & Requirements

Must-have

  • Biometrics vision and strategy for R&D
  • Innovative trial designs
  • AI applications in biostatistics
  • Liaising with Chinese regulatory
  • Statistical expertise for Therapy Areas
  • Timely delivery of high quality statistical deliverables
  • Managing local statisticians
  • Functional leadership and compliance
  • Technical and functional development of statisticians
  • Outreach to external institutions
  • Administrative and technical oversight
  • Senior thought partner to R&D leadership
  • Develop people including recruitment and retention
  • Foster a culture of scientific excellence
  • Statistical analyses for clinical trial results
  • Collaborative strategic partners with scientific colleagues
  • Influence content of regulatory guidelines

Nice-to-have

  • Strong awareness of NMPA, EU and US regulatory
  • Team-working skills and clear communication
  • Good time management and organizational skills
  • Continuous improvement
  • Speed and quality in data analyses

Key Requirements

  • Extensive clinical development and business experience
  • Thorough understanding of clinical, regulatory and marketing operations
  • Leadership, project management, resource management capabilities
  • Effective verbal and written communication skills
  • Experience supporting regulatory submissions
  • At least 7 years of experience managing complex projects
  • At least 3 years staff management experience
  • Demonstrated project management and budget management expertise

Work Rights

Not specified

Tailored Resume

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