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Responsibilities:
- Provide statistical expertise for the design, analysis, and reporting of clinical and/or preclinical studies
- Partner with cross-functional teams on study design, protocol development, and selection of appropriate statistical methodologies
- Develop statistical analysis plans and detailed analysis specifications
- Collaborate with statistical programming to ensure analyses are executed according to defined plans and standards
- Work closely with data management and clinical operations to support high-quality data collection and database design
- Contribute to data interpretation, reporting, and preparation of scientific materials and publications
- Support the development and refinement of departmental standards, SOPs, and templates
- Represent the biostatistics function on cross-functional project teams
- PhD in Biostatistics, Epidemiology, or a related quantitative field
- Minimum of 5 years of industry experience in a biostatistics role within life sciences
- Experience supporting early-phase clinical studies (e.g., Phase I–II), preferably in complex therapeutic areas
- Strong ability to work both independently and collaboratively in a team environment
- Excellent written and verbal communication skills
- Solid interpersonal and project coordination skills
- Proficiency in statistical programming tools such as SAS and/or R