Principal Statistical Programmer (Biotech)

Location: Onsite in Warren, New Jersey or Cambridge, Massachusetts

Salary: $109,900–$179,300 annually

Company

Biotechnology company developing and commercializing medicines for serious diseases across oncology, cardiovascular, neurological, infectious, rare, and other therapeutic areas.

What you will do

• Support or lead programming and quality control for clinical analysis datasets, tables, listings, and graphs.
• Create and maintain programming specifications for analysis datasets across studies.
• Design and independently test program logic while maintaining documentation in a regulated environment.
• Support submission requirements, including annotated CRFs and define documents.
• Coordinate timelines and milestones with multidisciplinary study teams through regulatory approval and launch.
• Contribute to presentations, statistical ad hoc requests, working groups, tool development, and process improvement.

Requirements

• Master’s degree and 3+ years of relevant experience.
• Programming experience supporting clinical study data and analysis deliverables.
• Strong documentation and quality control skills in a regulated environment.
• Experience collaborating with multidisciplinary study teams.
• Analytical problem-solving ability, attention to detail, and a quality-focused approach.
• Ability to work onsite in Warren, New Jersey or Cambridge, Massachusetts.

Culture & Benefits

• Science-driven work focused on developing life-changing medicines.
• Inclusive workplace and equal employment opportunity environment.
• Comprehensive rewards may include bonuses, equity awards, retirement benefits, 401(k) matching, insurance, paid time off, and family support benefits.
• Reasonable accommodations are available during recruitment for applicants with disabilities or chronic illnesses.

Hiring process

• Background checks may verify identity, right to work, and educational qualifications where required by local law.