Senior Biostatistics Lead - Trial Design & Strategy

0020 E.R. Squibb & Sons,L.L.C.; Princeton (NJ); On-site; USD 190,000 - 230,000; Full time

Benefits offered by this job

Wellbeing support

Retirement and financial protection

Insurance offerings

Job summary

Bristol Myers Squibb in Princeton, NJ seeks an experienced Associate Director of Biostatistics to join cross-functional Development teams and contribute to trial design, analysis planning, and regulatory submissions. The role collaborates with the Biostatistics indication Lead and other team members to advance assets, defend protocols, and present results clearly.

A PhD or MS in statistics/biostatistics with clinical trial experience and SAS/R/Python skills are required.

Qualifications

• PhD (6+ years) or MS (8+ years) in statistics/biostatistics with clinical trials experience.
• Proficiency in SAS, R or Python and advanced statistical analysis.
• Great interpersonal, communication, writing and organizational skills
• Expertise in statistical/clinical trials methodology for clinical development
• Good understanding of regulatory landscape and regulatory interactions

Responsibilities

• Collaborates in design of innovative and efficient clinical trials and study objectives.
• Defends protocols and analysis plans at governance reviews.
• Independently authors/reviews protocol, SAPs, reports and publications.
• Presents summary data and analyses results clearly and concisely.
• Provides statistical leadership for health authority requests and publications.
• Manages multiple studies within an indication or therapeutic area.

Skills

SAS

R

Python

Biostatistics

Education

PhD or MS in Statistics/Biostatistics

Tools

SAS

R

Python

Job description

Bristol Myers Squibb in Princeton, NJ seeks an experienced Associate Director of Biostatistics to join cross-functional Development teams and contribute to trial design, analysis planning, and regulatory submissions. The role collaborates with the Biostatistics indication Lead and other team members to advance assets, defend protocols, and present results clearly.

A PhD or MS in statistics/biostatistics with clinical trial experience and SAS/R/Python skills are required.