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As of Sep 9, 2026, the average yearly pay for global statistical programming director in the United States is $280,147.00, according to ZipRecruiter salary data. Most workers in this role earn between $260,500.00 and $322,500.00 per year, depending on experience, location, and employer.

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Infographic showing various Global Statistical Programming Director job openings in the United States as of August 2026, with employment types broken down into 83% Full Time, 11% Part Time, 5% Contract, and 1% Nights. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $280,147 per year, or $134.7 per hour.

Associate Director, Statistical Programming

Waltham, MA • On-site

Sironax Ltd.
See more jobs at Sironax Ltd.external

$125 - $150/hr

Other

Re-posted 4 days ago

Job description

Associate Director, Statistical ProgrammingAssociate Director, Statistical Programming

Waltham, Massachusetts, United States

Position Overview

Sironax is seeking a highly motivated and experienced Associate Director, Statistical Programming to play a critical leadership role within our global clinical development organization. This position combines strategic oversight with hands-on programming expertise, offering a unique opportunity to influence clinical development, regulatory submissions, and corporate milestones.

The ideal candidate is adaptable, collaborative, and thrives in a fast-paced biotech environment. You will oversee CRO programming deliverables while also supporting high-priority internal analyses, executive presentations, and regulatory reporting activities across multiple therapeutic areas, including rare diseases.

Key Responsibilities
  • Lead oversight and management of CROs and external vendors to ensure timely, high-quality delivery of SDTM, ADaM, and TFL outputs.
  • Provide hands-on statistical programming support for internal analyses, executive presentations, investor materials, and regulatory submissions.
  • Collaborate closely with cross-functional teams including Biostatistics, Clinical Operations, Data Management, Regulatory Affairs, and Investor Relations.
  • Maintain alignment across global teams, including effective collaboration with US- and China-based stakeholders across multiple time zones.
  • Ensure compliance with CDISC standards, FDA/EMA regulatory requirements, and industry best practices.
  • Support programming activities across a diverse clinical pipeline, including complex and data-limited rare disease programs.
  • Contribute to process improvement initiatives, programming standards, and operational efficiencies within the statistical programming function.
Qualifications
  • Bachelor’s or Master’s degree in Statistics, Biostatistics, Computer Science, Mathematics, or a related quantitative discipline.
  • Minimum of 8 years of statistical programming experience within the biotechnology or pharmaceutical industry.
  • At least 2 years of leadership, vendor oversight, or project management experience.
  • Advanced proficiency in SAS programming; experience with R programming is highly desirable.
  • Strong knowledge of CDISC standards (SDTM and ADaM) and regulatory submission requirements.
  • Experience supporting regulatory submissions and corporate milestones such as investor presentations or fundraising activities is preferred.
  • Excellent communication and collaboration skills with the ability to work effectively in a global environment.
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