Lead Statistical Programmer, Clinical Trials & Submissions

Terumo Aortic; Town of Florida (NY); On-site; USD 140,000 - 190,000; Full time

Job summary

Terumo Aortic is seeking a Senior Statistical Programmer to develop, validate, and document statistical analysis programs for clinical trial data and regulatory submissions, leading programming activities and mentoring junior staff.

You will collaborate with biostatisticians, data managers, and cross-functional teams to ensure timely delivery of high-quality outputs (tables, listings, figures) and drive process improvements that enhance data quality and compliance.

Qualifications

• Bachelor’s degree in a scientific or related discipline and strong SAS programming experience.
• Extensive SAS programming experience in pharmaceutical, biotechnology, CRO, or medical device settings.

Responsibilities

• Perform and support statistical programming activities for clinical trial datasets (SDTM/ADaM) and outputs, ensuring timely, high-quality deliverables.
• Conduct quality control checks and peer code reviews to ensure accuracy and regulatory compliance.
• Collaborate with biostatisticians, data managers, and cross-functional teams to meet project timelines and quality expectations.
• Lead programming activities for device types or therapeutic areas, coordinate multiple projects, and mentor junior programmers.
• Review SAPs, mock TLF shells, specifications, CRFs, and database design, providing proactive feedback to optimize efficiency and data quality.
• Drive process improvements and standardization to increase department efficiency.

Skills

Statistical programming

SAS programming

Quality assurance

Mentoring

Cross-functional collaboration

Education

Bachelor's degree in a scientific or related discipline

Tools

SAS

R

Job description

Terumo Aortic is seeking a Senior Statistical Programmer to develop, validate, and document statistical analysis programs for clinical trial data and regulatory submissions, leading programming activities and mentoring junior staff.

You will collaborate with biostatisticians, data managers, and cross-functional teams to ensure timely delivery of high-quality outputs (tables, listings, figures) and drive process improvements that enhance data quality and compliance.