Senior Biostatistics Lead for Oncology Trials

Relay Therapeutics

Cambridge (MA)

On-site

USD 160,000 - 228,000

Full time

6 days ago
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Job summary

Relay Therapeutics is seeking an Associate Director of Biostatistics to lead statistical activities across clinical studies and maintain data integrity. You will guide SAS/R analyses, oversee timelines, and collaborate with cross-functional teams to ensure robust trial design and reporting.

The role emphasizes expert statistical methods, CDISC SDTM/ADaM knowledge, and clear communication of complex results to non‑statisticians. Oncology experience is valued in a dynamic biotech environment.

Qualifications

  • PhD in statistics, biostatistics, or related field.
  • 6+ years of pharmaceutical/biotech statistics experience.
  • Oncology experience preferred.
  • Strong programming using SAS or R.
  • Knowledge of CDISC SDTM/ADaM models.
  • Experience with CRO/vendor oversight.

Responsibilities

  • Lead biostatistics for a clinical program and advise on statistical activities.
  • Oversee day-to-day biostatistics work, timelines and deliverables.
  • Contribute to protocol development, SAP, and clinical study reports.
  • Apply advanced statistics for innovative trial designs and data displays.
  • Ensure rigorous statistical methodology and scientific integrity.
  • Collaborate with Clinical Operations, RD&D, Regulatory, and other teams.
  • Support regulatory submissions, briefing books, and integrated summaries.
  • Support presentations and publications of trial results.
  • Help develop department SOPs and standard practices.
  • Assist Head of Biostatistics with budgeting and resourcing.

Skills

SAS
R
Statistical analysis
Communication

Education

PhD in statistics/biostatistics

Tools

CDISC SDTM/ADaM

Job description

Relay Therapeutics is seeking an Associate Director of Biostatistics to lead statistical activities across clinical studies and maintain data integrity. You will guide SAS/R analyses, oversee timelines, and collaborate with cross-functional teams to ensure robust trial design and reporting.

The role emphasizes expert statistical methods, CDISC SDTM/ADaM knowledge, and clear communication of complex results to non‑statisticians. Oncology experience is valued in a dynamic biotech environment.

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