Associate Director, Biostatistics & Trial Strategy

Bristol Myers Squibb; Madison (NJ); On-site; USD 190,000 - 230,000; Full time

Job summary

Bristol Myers Squibb in Madison, New Jersey is seeking an Associate Director, Biostatistics to join cross-functional development teams, contributing to trial design, analysis planning, and regulatory submissions.

The role involves leading statistical activities, collaborating across indications, providing scientific leadership, and mentoring team members, with emphasis on regulatory interactions and quality deliverables.

Qualifications

• PhD (6+ years) or MS (8+ years) in statistics or biostatistics with clinical trials or drug development experience.
• Proficiency in SAS, R or Python and implementation of advanced statistical analyses.
• Excellent interpersonal, communication, writing and organizational skills.
• Expertise in statistical/clinical trials methodology and regulatory experience.
• People manager experience is preferred (for people manager position only).

Responsibilities

• Collaborates in design of innovative and efficient clinical trials and study objectives.
• Authors or reviews protocols, SAPs, and study reports.
• Presents data and analyses clearly to stakeholders.
• Provides statistical leadership for health authority interactions.
• Manages multiple studies ensuring standards and consistency.

Skills

Statistical analysis

Clinical trials

Regulatory awareness

Leadership

Communication

Education

PhD in statistics/biostatistics

MS in statistics/biostatistics

Tools

SAS

R

Python

Job description

Bristol Myers Squibb in Madison, New Jersey is seeking an Associate Director, Biostatistics to join cross-functional development teams, contributing to trial design, analysis planning, and regulatory submissions.

The role involves leading statistical activities, collaborating across indications, providing scientific leadership, and mentoring team members, with emphasis on regulatory interactions and quality deliverables.