Manager, Statistical Programming, Pharmacometrics

Scorpion Therapeutics; Village of Tarrytown (NY); On-site; USD 150,000 - 230,000; Full time

Benefits offered by this job

Four‑day workweek

On-site in Tarrytown, NY

Job summary

Scorpion Therapeutics is seeking a Manager of Pharmacometrics Programming to lead advanced statistical programming for pharmacometrics analyses in support of clinical development. You will manage datasets, tables, figures, and submission documents, ensuring QC and adherence to CDISC standards.

The role emphasizes collaboration with cross-functional teams, delivering high-quality trial reports, and driving process improvements.

Qualifications

• Bachelor’s degree required; Master’s preferred; 7–9+ years of statistical programming in pharma.

Responsibilities

• Lead programming activities for datasets, tables, figures across trials.
• Ensure quality control; develop and validate programming specifications.
• Integrate data for pharmacokinetics and pharmacometric analyses; exposure–response.
• Support regulatory submissions, scientific publications and presentations.
• Lead creation of electronic submission documents; partner with cross-functional teams.
• Drive process improvements and standards across the team.

Skills

Advanced SAS

Pharmacometrics

PK/PD

CDISC

Project management

Communication

Cross-functional collaboration

Regulatory submissions

Data integration

Education

Bachelor's degree (Master's preferred)

Tools

SAS

Job description

Role: Manager, Pharmacometrics Programming, supporting clinical development with advanced statistical programming and analyses.

Responsibilities

lead programming activities for datasets, tables, figures; ensure quality control; develop and validate programming specifications; integrate data for pharmacokinetics and pharmacometric analyses; support regulatory submissions, scientific publications, and presentations; lead creation of electronic submission documents; partner with cross-functional teams to deliver high-quality trial reports; drive process improvements and standards.

Requirements

Bachelor's degree (Master's preferred); 7-9+ years in statistical programming within pharma or regulatory environment; advanced SAS expertise; strong understanding of pharmacometrics (PK, PD, exposure-response); experience supporting clinical reporting and regulatory standards (CDISC); excellent project management, communication, and collaboration skills.

High-Value

clinical pharmacology, pharmacometric analyses, regulatory submissions, SAS programming, cross-functional collaboration, on-site in Tarrytown, NY, with a four-day workweek.