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Commission Director Statistical Programming Jobs

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Associate Director, Statistical Programming

The Associate Director, Statistical Programming works closely with the Executive Director, Statistical Programming and other members of the Biometrics team to provide programming support across all ...

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As of Aug 20, 2026, the average yearly pay for commission director statistical programming 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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Commission Director Statistical Programming jobs near you
Infographic showing various Commission Director Statistical Programming job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 9% Part Time, and 5% Contract. Highlights an 67% Physical, 1% Hybrid, and 32% Remote job distribution, with an average salary of $280,147 per year, or $134.7 per hour.

Associate Director, Statistical Programming

Sironax Ltd.

Waltham, MA • On-site

$120 - $150/hr

Other

Posted 15 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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