FSP Principal Biostatistician, Phase 2 and 3

What you’d do

Provides statistical support for Phase 2 and 3 pharmaceutical clinical trials, including sample size and power calculations, authoring statistical analysis plans, and validating efficacy and safety analysis datasets and TLFs. Also supervises programmers and supports IND or NDA activities. Found on the employer's careers page on Oct 18, 2026. Apply through the link.

You’ll need

• PhD in statistics or biostatistics with 3+ years industry experience, or MS with 5+
• 2+ years Phase 2/3 clinical trial experience
• Statistical analysis plan authoring
• SAS/statistical programming and TLF validation
• IND/NDA support experience