Senior Manager, Biostatistics

Scorpion Therapeutics; California (MO); On-site; USD 150,000 - 190,000; Full time

Job summary

Gilead Sciences is seeking a Biostatistics lead to support clinical studies and non‑molecule projects within its biopharma portfolio. You will lead statistical analyses, advise on study design, and author analysis plans while overseeing technical activities across multiple projects.

The role involves collaboration on trial design, data analysis, safety monitoring, and regulatory documentation, with opportunities to influence NDA submissions and biomarker analyses in a dynamic, cross‑functional

Qualifications

• PhD preferred or MS/BA with substantial industry experience.
• Strong background in biomedical data analysis and statistical methods.
• Experience supporting NDA submissions and regulatory data packages.

Responsibilities

• Statistical analysis across clinical studies and non-molecule projects.
• Study design consultation with cross‑functional teams.
• Authoring and reviewing analysis plans and documentation.
• Overseeing technical activities and project execution.
• Contributing to regulatory submissions and data interpretation.
• Leading projects on statistical tools and methods.

Skills

Statistical analysis

Study design

Authoring analysis plans

Overseeing technical activities

Regulatory documentation

Education

PhD (preferred)

MS/BA with 4+ to 8+ years' industry experience

Tools

SAS

Job description

Role: Biostatistics lead supporting clinical studies and non-molecule projects within Gilead's biopharma portfolio.

Responsibilities

• Statistical analysis
• Study design consultation
• Authoring analysis plans
• Overseeing technical activities
• Contributing to NDA submissions
• Cross‑functional collaboration on trial design, data analysis, safety monitoring, and regulatory documentation
• Leading projects related to statistical tools and methods

Requirements

• PhD (preferred) or MS/BA with 4+ to 8+ years' industry experience
• Expertise in biomedical data analysis using SASProven project/team management skills

High‑value: supports clinical development across infectious diseases, oncology, and other therapeutic areas; involved in preclinical, IND, or phase 1-3 trials; may include biomarker and safety analyses.

The position offers matrix management, regulatory compliance, and potential leadership in special projects.

Work setup is not specified, but the emphasis on collaboration and project oversight indicates a dynamic, cross‑functional environment.