Director, Statistical Programming, Pharmacometrics

Scorpion Therapeutics; Village of Tarrytown (NY); On-site; USD 180,000 - 260,000; Full time

Job summary

Scorpion Therapeutics seeks a Lead for strategic pharmacometrics programming across clinical development programs, supporting data analysis, regulatory submissions, and departmental standardization.

You will oversee programming strategies, mentor teams, and ensure CDISC-compliant deliverables while coordinating with cross-functional teams; on-site in Tarrytown, NY, four days per week.

Qualifications

• Master's degree required in Statistics, Computer Science, Mathematics, Engineering, or related field.
• 12+ years of experience supporting clinical trial data in biotech or pharma.
• Expert SAS programming skills.
• Experience leading teams of 4+.

Responsibilities

• Oversee programming strategy; implement tools and methods; coordinate cross-functional activities; manage data integration for pharmacometric analyses; validate submissions.

Skills

Pharmacometrics

SAS programming

Leadership

Biostatistics

Regulatory submissions

CDISC standards

Clinical reporting

Data integration

Education

Master's degree in Statistics/CS/Math/Engineering

Tools

SAS

Job description

Role: Lead strategic pharmacometrics programming for clinical development programs across multiple therapeutic areas, supporting data analysis, regulatory submissions, and departmental standardization.

Responsibilities

• oversee programming strategies, implement tools and methodologies, coordinate activities with cross-functional teams, manage data integration for pharmacometric analyses, validate electronic submission deliverables, develop talent, and drive process improvements.

Requirements

• Master's degree in Statistics, Computer Science, Mathematics, Engineering, or related field;
• 12+ years supporting clinical trial data in biotech or pharma;
• expert SAS programming skills;
• experience leading teams of 4+;
• strong understanding of pharmacometrics, biostatistics, clinical reporting, and regulatory standards;
• experience with CDISC standards.

Preferred

• SAS Certification.

HighValue

• extensive SAS expertise in clinical development, leadership experience, and knowledge of regulatory submission processes.

WorkSetup

On-site in Tarrytown, NY, four days/week.