About this role
Director, Biostatistics at Alnylam. Location: Cambridge or United States. Role: leading programs, designing trials, authoring protocols Requirements: Ph.D. (preferred) with 8+ years pharma statistics experience; expertise in late‑phase clinical trial design, Bayesian/adaptive methods, NDA/MAA submissions, proficiency in SAS and R, ADaM and eCRF design, strong communication and leadership. Category: Research and Development (R&D) Seniority: Senior Level Tools: SAS, R, ADaM, eCRFs Commitment: Full Time Workplace: Hybrid Languages: English