Lead Pharmacometrics Statistical Programmer (Onsite 4 Days/Week)

BioSpace; Village of Tarrytown (NY); On-site; USD 129,000 - 210,000; Full time

Job summary

Regeneron in Tarrytown, NY, is seeking a senior Statistical Programmer to lead programming and QC across multiple projects. This on-site role involves coordinating pharmacometrics activities with cross‑functional teams and stakeholders.

You will create, maintain, and validate programming specifications, integrate study data for PK/PD analyses, and support regulatory deliverables, publications, and conferences. Strong project management and collaboration skills are essential.

Qualifications

• Advanced SAS programming in a clinical/pharma setting.
• Strong pharmacometrics knowledge incl PK, exposure‑response, population PK.
• Experience supporting clinical study reporting and regulatory deliverables.
• Familiarity with CDISC data standards.
• Excellent project management, communication, and cross‑functional collaboration.

Responsibilities

• Lead programming and quality control activities for analyses across multiple projects.
• Coordinate pharmacometrics programming with cross‑functional teams and stakeholders.
• Create, maintain, and validate programming specifications for standardized analyses.
• Integrate data across studies to support exposure‑response and population PK analyses.
• Support regulatory requests, data‑driven analyses, publications, and conferences.
• Lead creation and validation of electronic submission deliverables and docs.
• Partner with multidisciplinary study teams to deliver high‑quality analyses and reports.
• Drive process improvements, standards development, and departmental initiatives.

Skills

SAS programming

Pharmacometrics analyses

CDISC data standards

Project management

Communication

Problem solving

Cross-functional collaboration

Education

Bachelor's degree

Master's degree

Job description

Regeneron in Tarrytown, NY, is seeking a senior Statistical Programmer to lead programming and QC across multiple projects. This on-site role involves coordinating pharmacometrics activities with cross‑functional teams and stakeholders.

You will create, maintain, and validate programming specifications, integrate study data for PK/PD analyses, and support regulatory deliverables, publications, and conferences. Strong project management and collaboration skills are essential.