What you'll do:
As a Biostatistician , you will play a critical role in advancing our clinical programs by applying statistical expertise to complex biological and clinical data. Your contributions will directly impact data-driven decision-making in a fast-paced, cutting-edge biotech environment.

• Provide statistical expertise for clinical study design, data analysis, and interpretation to drive data-driven decisions.
• Develop and review statistical analysis plans (SAPs), programming specifications, and data visualizations to support clinical trials and regulatory submissions.
• Collaborate cross-functionally with clinical, data science, regulatory, and biometrics teams to ensure high-quality, reproducible results.
• Act as a key contributor for regulatory submissions , including interactions with the FDA and other global health authorities.
• Support real-world data analysis and machine learning-driven insights , integrating traditional biostatistics with an AI-driven approach.
• Mentor junior team members and help maintain best practices for statistical methodologies within the organization.

What You Bring:

• PhD in Biostatistics, Statistics, or a related field with 3+ years of experience , or a Master's degree with 5+ years of experience in Biostatistics.
• Strong background in clinical trial design, Bayesian modeling, adaptive trials, and/or biomarker-driven analysis .
• Experience in biotech, pharma, or CRO environments, with a preference for candidates familiar with early-phase clinical trials.
• Proficiency in SAS and R , with experience in high-dimensional data analysis or AI/ML-enhanced analytics being a plus.
• Strong problem-solving skills, adaptability, and ability to work in a dynamic, evolving environment.
• Excellent communication and collaboration abilities , with experience presenting statistical results to cross-functional teams.

If this sounds like the role for you and you're interested in taking the next steps, reach out to: