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Director Statistical Programming Jobs in Canton, MA

Head of Biometrics

Watertown, MA ยท On-site

$310K - $395K/yr

In your role as Head of Biometrics , you will be responsible for leading all biostatistics and statistical programming activities across Treeline's clinical and translational development programs.

Senior Director, Biostatistics

Waltham, MA ยท On-site

$250 - $290/hr

Role Summary The Senior Director, Biostatistics provides strategic, technical, and operational ... Management, Statistical Programming, Translational Medicine, Program Management, and other ...

Senior Director, Biostatistics

Waltham, MA ยท Hybrid

$227K - $284K/yr

The Senior Director of Biostatistics is accountable for providing statistical leadership and ... Proficiency in SAS programming and other statistical software tools. * Ability to manage people and ...

... and experienced Associate Director, Biostatistics to play a critical role within our global ... Collaborate closely with cross-functional teams including Statistical Programming, Clinical ...

Biostatistics Director (Hybrid)

Boston, MA ยท Hybrid

$201K - $301K/yr

General Summary: The Director, Biostatistics will independently perform highly scientific ... Leads collaboration with statistical programming and other functions to ensure high quality and ...

Showing results 41-60

Director Statistical Programming information

See Canton, MA salary details

$162.3K

$296.2K

$363.7K

How much do director statistical programming jobs pay per year?

As of Aug 7, 2026, the average yearly pay for director statistical programming in Canton, MA is $296,229.00, according to ZipRecruiter salary data. Most workers in this role earn between $275,500.00 and $341,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a director statistical programming?

To thrive as a Director of Statistical Programming, you need advanced expertise in statistical analysis, programming languages such as SAS or R, and a strong background in clinical trial data, typically supported by a degree in statistics, mathematics, or a related field. Familiarity with regulatory submission processes, CDISC standards, and project management tools is essential, as are relevant certifications like SAS Certified Professional. Leadership, effective communication, and strategic thinking are key soft skills for managing teams and collaborating across departments. These skills ensure high-quality data outputs, regulatory compliance, and successful execution of complex clinical development projects.

What is a director statistical programming?

The job of a director of statistical programming oversees the development and implementation of SAS programs to produce statistical analysis datasets. In this career, your responsibilities include managing the team that generates tables and graphs using the SAS programs for applications such as clinical studies. Other duties include participating in the planning and review of statistical analysis and studying reports, abstracts, and manuscripts as required. You collaborate with project leads to contribute to department operations and standards, such as CDISC for clinical research.

How does a director statistical programming typically collaborate with cross-functional teams in a pharmaceutical or biotech company?

A Director of Statistical Programming regularly works with biostatistics, clinical data management, regulatory affairs, and medical writing teams to ensure that statistical deliverables meet project timelines and regulatory requirements. They coordinate programming efforts across multiple studies, provide leadership and mentorship to programming staff, and help resolve technical or resource-related challenges. Effective collaboration is essential to streamline workflows, maintain data integrity, and ensure clear communication of statistical results within the organization.

What does a director statistical programming do?

A Director of Statistical Programming oversees teams responsible for the programming and analysis of clinical trial data, ensuring the accuracy and integrity of statistical outputs. They set departmental strategies, manage resources, and ensure compliance with regulatory requirements and industry standards. This role also involves collaborating with other departments, such as biostatistics and clinical operations, to support the successful delivery of statistical analyses for drug development and regulatory submissions. They play a key leadership role in mentoring staff and advancing programming processes and technologies.
What job categories do people searching Director Statistical Programming jobs in Canton, MA look for? The top searched job categories for Director Statistical Programming jobs in Canton, MA are:
What cities near Canton, MA are hiring for Director Statistical Programming jobs? Cities near Canton, MA with the most Director Statistical Programming job openings:
Infographic showing various Director Statistical Programming job openings in Canton, MA as of July 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, 1% Temporary, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $296,229 per year, or $142.4 per hour.

Head of Biometrics

Treeline Biosciences

Watertown, MA โ€ข On-site

$310K - $395K/yr

Other

Re-posted 10 days ago


Job description

In your role as Head of Biometrics, you will be responsible for leading all biostatistics and statistical programming activities across Treeline's clinical and translational development programs. This includes ownership of statistical strategy, clinical trial design, statistical analysis planning, and interpretation of results for regulatory submissions, publications, and decision-making. You will build and manage internal and external biometrics capabilities and ensure the delivery of high-quality, timely, and compliant data outputs to support the advancement of the company's development pipeline. In close collaboration with clinical development, data management, translational sciences, and regulatory affairs, you will play a critical role in ensuring scientifically rigorous and data-driven development strategies.

Key Responsibilities:

  • Lead and own the statistical strategy across all stages of clinical development, from study design through regulatory submission.
  • Provide statistical leadership for protocol design, randomization, sample size determination, and analysis plans.
  • Oversee and review statistical deliverables including SAPs, TFLs, integrated summaries, and ad hoc analyses.
  • Collaborate with cross-functional teams to ensure alignment of biometrics strategy with clinical and regulatory goals.
  • Serve as the company's statistical expert in regulatory interactions and ensure compliance with global regulatory standards (FDA, EMA, ICH).
  • Leadย  development of data visualizations, dashboards, analyses, and presentation-ready outputs to support internal decision-making and external presentations for governance meetings, scientific meetings, regulatory interactions, and external partner discussions.
  • Manage the statistical programming function and ensure delivery of high-quality datasets and analysis outputs in support of study reports, submissions, and publications.
  • Build and lead a high-performing internal biometrics team while managing outsourced CRO partners and statistical consultants.
  • Provide leadership in establishing standard operating procedures and data governance best practices for biometrics.
  • Help shape the broader data strategy and analytics infrastructure in collaboration with clinical data management, clinical operations, and IT.

Required Qualifications:

  • Advanced degree in Biostatistics, Statistics, Mathematics, or a related field
    • PhD + >10 years relevant industry experience
    • MS + >15 years relevant industry experience
  • Proven experience leading biostatistics and/or biometrics functions in biotech or pharmaceutical settings.
  • Strong knowledge of statistical methodology, clinical trial design, and regulatory requirements.
  • Hands-on experience with oncology clinical development strongly preferred.
  • Demonstrated success managing external vendors and building biometrics infrastructure in a fast-paced environment.
  • Strong communication skills with the ability to translate complex statistical issues to non-technical audiences.
  • Foster a collaborative, solutions-oriented biometrics organization focused on responsiveness, quality and support of stakeholder requests - or serve as strategic partner to senior leadership team, delivering timely biometrics insights and presentation support for high-priority and time-sensitive initiatives.ย 
  • Strategic thinker with attention to detail, leadership presence, and a commitment to scientific rigor.

This position is classified as exempt. The anticipated annual base salary range for candidates who will work in Watertown, MA is $310,000 - $395,152. The final base salary offered to the successful candidate will be dependent upon several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the job, education, and other factors. Treeline Biosciences is a multi-state employer, and this salary range may not reflect positions that work in other cities or states.

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