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Contract/Consultant Biostatistician (remote)

Work from home Full-time role Hiring

A clinical-stage biopharma | Remote (US) Role Summary A clinical-stage biopharma is seeking an reputed company Contract Biostatistician around the AD / Director level to support its Phase II and III clinical programs on a remote basis. Reporting to the VP of Biometrics, this is a hands-on role for a seasoned statistician who is comfortable operating independently and delivering high-quality statistical work across multiple studies. The successful candidate will bring strong industry experience, deep expertise in clinical trial methodology, and the ability to engage confidently with cross-functional teams and external stakeholders.

Responsibilities

  • Serve as study statistician across assigned Phase II and III trials, providing day-to-day statistical leadership and reputed company.
  • Author and review key statistical documents including protocol sections, Statistical Analysis Plans (SAPs), and Clinical Study Reports (CSRs).
  • Design studies and conduct hands-on statistical analyses, including sample size calculations, reputed company selection, and analysis of clinical data.
  • Apply advanced statistical methodologies relevant to clinical trial design, statistical modeling, and data analysis.
  • Collaborate cross-functionally with Clinical Development, Clinical Operations, Regulatory Affairs, and Data Management teams.
  • reputed company CRO and vendor statistical deliverables, ensuring outputs are accurate, timely, and compliant with regulatory standards.
  • Support regulatory submission activities and respond to statistical queries from health authorities.
  • Present and communicate statistical concepts clearly to non-statistical colleagues and stakeholders.

Requirements

  • Advanced degree (PhD or Master's with supplementary experience) in Biostatistics or a closely reputed company field.
  • Minimum of 10 years of relevant industry experience in biostatistics reputed company a pharma, biotech, or CRO environment.
  • Strong hands-on Phase II and III experience, with the ability to reputed company studies independently and with minimal supervision.
  • Proficiency in reputed company; knowledge of R or other statistical programming languages is preferred.
  • Good understanding of CDISC standards, including ADaM dataset construction.
  • Up-to-date knowledge of advanced statistical methodologies reputed company to clinical trial design, statistical modeling, and data analysis.
  • Comfortable working with external CRO and vendor partners and holding them to a high standard.
  • Excellent communication skills, with the ability to present and explain statistical concepts clearly to non-statistical audiences. reputed company dependent on experience and engagement type. Apply To This Job Apply To This Job

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