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Focusing on clinical trial design and analysis, the full-time Associate Director of Biostatistics will collaborate with cross-functional teams to develop protocols, manage multiple studies, and provide statistical leadership while working onsite in various locations including Princeton, Seattle, Brisbane, and Cambridge Crossing.
Key Responsibilities: Collaborates in the design of innovative clinical trials and contributes to project development strategy Independently authors and reviews statistical analysis plans, clinical study reports, and related documents Manages multiple studies to ensure adherence to standards within a specific indication or therapeutic area
Required Qualifications: PhD in statistics or biostatistics with 6+ years of experience, or MS with 8+ years of relevant experience Proficiency in scientific computing/programming (SAS, R, or Python) and advanced statistical analysis Expertise in statistical/clinical trials methodology related to clinical development Good understanding of the regulatory landscape and experience with regulatory interactions Demonstrated leadership abilities and project management skills

Also on the board Same function, level within a rung

Level

Lead

Location

Denver, CO

Occupation

Biostatisticians

Industry

Research and Development in Biotechnology

Posted

today

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