Director, Biostatistics

About Altimmune:

Altimmune (NASDAQ: ALT) is a late clinical-stage biopharmaceutical company developing therapies for patients with serious liver diseases. The Company’s lead candidate, pemvidutide, is a unique dual‑action therapy targeting both glucagon and GLP‑1 receptors in a balanced 1:1 ratio in development for the treatment of metabolic dysfunction‑associated steatohepatitis (MASH), alcohol use disorder (AUD), and alcohol‑associated liver disease (ALD). For more information, please visit

Job Position
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This is a high‑visibility, high‑impact role that will be critical to Altimmune’s growth. Reporting to the Senior Director, Biostatistics, this individual will provide statistical leadership and serve as the lead statistician for one or more clinical development programs within Altimmune’s pipeline. The role involves collaborating with clinical and development teams, including clinicians, clinical scientists, statistical programmers, data managers, regulatory, and clinical operations professionals, to plan, conduct, and analyze clinical studies of all phases.

Responsibilities include ensuring the overall quality of statistical design, programming, analysis, and data reporting, representing the company in interactions with external statistical and data management service providers, and participating in discussions with regulatory agencies.

Workplace Designation
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Depending upon location, this role will be hybrid or remote and will require some travel as business needs dictate.

• Serve as the lead statistician for one or more clinical development programs, providing statistical and operational leadership across all phases of clinical research.
• Provide statistical input into development strategy, study design, sample size determination, endpoint selection, estimands, and analysis methodology.
• Perform or oversee statistical analyses for interim study results, database locks, top‑line results, and final clinical study reports.
• Evaluate and implement innovative statistical methodologies, technologies, and AI‑enabled tools to improve efficiency and quality across clinical development.

• Develop and review statistical sections of clinical protocols, Statistical Analysis Plans (SAPs), Case Report Forms (CRFs), Clinical Study Reports (CSRs), and other regulatory documents.
• Ensure all statistical activities comply with ICH‑GCP guidelines, CDISC standards, regulatory guidance, and company standards.
• Contribute to the interpretation of clinical trial results and support the preparation of regulatory submissions, publications, scientific presentations, and responses to health authorities.
• Represent Altimmune in interactions with external statistical vendors, CROs, and regulatory agencies.

• Collaborate closely with Clinical Development, Clinical Operations, Data Management, Statistical Programming, Medical Affairs, and Regulatory Affairs to ensure high‑quality study design and execution.
• Work closely with statistical programmers to ensure timely development of analysis datasets, tables, listings, and figures (TLFs) supporting clinical development and regulatory submissions.
• Review and validate statistical programming deliverables, programmatically or through independent review, as appropriate.
• Oversee statistical activities performed by CROs and external vendors, ensuring quality, timeliness, and compliance with regulatory requirements.

• Foster a culture of scientific rigor, collaboration, innovation, and continuous learning within the Biometrics organization.
• Contribute to departmental process improvements, standards development, and cross‑functional initiatives that strengthen Altimmune’s clinical development capabilities.

• PhD in Statistics, Biostatistics, or related field with 7+ years of clinical trial statistics experience in biotech/pharma; or MS with 10+ years of equivalent industry experience.
• Strong knowledge of statistical methods relevant to clinical trials, including longitudinal data, survival analysis, and Bayesian…