[R&D] Statistician, バイオメトリクス・データマネジメント統括部 統計担当者
Pfizer · Tokyo, Japan
BiometricsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Statistician role supporting clinical trial design, analysis, and interpretation within drug development. Position requires advanced statistical expertise, regulatory knowledge, and cross-functional collaboration with clinical development teams and global colleagues.
What they're looking for
- Master's degree or higher in statistics, biostatistics, or related field
- Strong statistical skills applied to clinical trials and post-marketing surveillance
- Broad understanding of pharmaceutical drug development processes
- Knowledge of clinical medicine and regulatory requirements
- Fluent written and oral English communication with international colleagues
- Cross-functional leadership and consulting abilities
- Effective verbal and written communication skills
What you'll be doing
- Provide statistical input on study design, analysis plans, and interpretation of clinical trial results
- Plan and deliver statistical analyses, topline reports, and clinical study reports for regulatory submissions
- Ensure compliance of all statistical activities with regulatory requirements and company standards
- Collaborate with clinical teams, data managers, and programmers on assigned studies and submissions
- Communicate with global therapeutic area statisticians and contribute to regulatory interactions
Privacy & handoff
This role links to Pfizer's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.