Associate Director, Biostatistics
Core
Design clinical trials, develop analysis plans, interpret results, and prepare regulatory submissions for drug development assets.
Role type
Senior individual contributor biostatistician (Associate Director)
Builds
Clinical study reports, statistical analysis plans, and regulatory submissions
Domain
Pharmaceutical clinical development / Biostatistics
Required skills
Clinical trial design, statistical analysis planning, regulatory submission preparation, SAS/R/Python, statistical methodology, project management
Preferred skills
Cross-functional collaboration, team leadership, scientific computing, regulatory landscape knowledge
Technologies
SAS, R, Python
Responsibilities
Collaborate on innovative clinical trial design and project development strategy; Defend protocols and analysis plans at internal governance reviews; Author and review study-level documents including clinical study reports; Present summary data and analysis results; Provide statistical support for health authority requests and publications; Manage multiple studies to ensure adherence to standards; Develop and advise team members.
Seniority
Senior, hands-on IC with leadership responsibilities