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Protocol Intelligence
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Job Description
Structured overview of role & requirementsAbout This Role
Lead statistical strategy and study design across all stages of medicine development to influence key product decisions and regulatory submissions.
Own and deliver statistical content including design, analysis plans, and interpretation with emphasis on benefit-risk and uncertainty quantification.
Provide global leadership by mentoring statisticians, partnering with CROs, representing the company externally, and influencing internal governance and investment decisions.
Minimum Requirements
Minimum 12+ years experience as a Statistician in pharma or healthcare industry.
Expertise in clinical trial protocol development, regulatory interactions, complex statistical computation, and decision making in drug development.
Proven leadership experience or recognized expertise at national level as a statistical technical expert.
Work Experience Required: Minimum 12+ years in pharma/healthcare statistics.
Ideal Candidate Profile
Experienced leader who can operate at executive governance levels and influence cross-functional teams and external collaborators including health authorities.
Deep methodological knowledge including adaptive designs, Bayesian methods, and advanced trial design with practical implementation skills.
Strong track record in delivering high-impact statistical strategy across multiple therapy areas and interfacing with payers and health technology assessment bodies.