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Associate Statistical Programmer Jobs in Massachusetts

Sironax

Associate Director, Biostatistics

Waltham, MA · On-site

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

Vrtx

Biostatistics Associate Director (HYBRID)

Boston, MA · Hybrid

$174K - $262K/yr

Biostatistics Associate Director will perform sophisticated scientific statistical analyses in ... Collaborates with statistical programming and other functions to ensure timely delivery of TFLs ...

PACE Industries

CMM Programmer

Billerica, MA · On-site

$36 - $44/hr

Interpret complex inspection results and statistical data (SPC), communicating variations or ... associates to corporate leadership. * Software: High proficiency in Microsoft Office Suite (Excel ...

Pace Industries

CMM Programmer

Billerica, MA · On-site

$36 - $44/hr

Interpret complex inspection results and statistical data (SPC), communicating variations or ... associates to corporate leadership. * Software: High proficiency in Microsoft Office Suite (Excel ...

Medicus Economics

Associate (ITC)

Boston, MA · On-site

Program analytic components in R and other statistical programming languages. * Qualitatively and ... Associates work on diverse projects, gain early responsibility, and contribute meaningfully to ...

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All JobsAssociate Statistical Programmer JobsAssociate Statistical Programmer Jobs in Massachusetts

Associate Statistical Programmer information

See Massachusetts salary details

$92.3K

$160.9K

$271.9K

How much do associate statistical programmer jobs pay per year?

As of Jul 13, 2026, the average yearly pay for associate statistical programmer in Massachusetts is $160,861.00, according to ZipRecruiter salary data. Most workers in this role earn between $136,500.00 and $174,700.00 per year, depending on experience, location, and employer.

What is an Associate Statistical Programmer?

An Associate Statistical Programmer is an entry-level professional who assists in the programming and analysis of clinical trial data, primarily within the pharmaceutical or biotechnology industries. They use statistical software, such as SAS or R, to create, validate, and maintain datasets, tables, listings, and figures required for clinical study reports. Their work supports biostatisticians and clinical teams in ensuring data accuracy and regulatory compliance. This role is ideal for those with a background in statistics, mathematics, or computer science, looking to start a career in clinical data analysis.

How does an Associate Statistical Programmer typically collaborate with biostatisticians and data managers in clinical research projects?

As an Associate Statistical Programmer, you will frequently collaborate with biostatisticians to understand statistical analysis plans and translate them into clear programming specifications. You’ll also work closely with data managers to ensure data integrity and resolve any data discrepancies before analysis. Effective communication and teamwork are essential, as you’ll often participate in project meetings, provide programming support, and help deliver high-quality datasets and reports under tight timelines. This collaborative environment is key to ensuring accurate and timely clinical trial results.

What is the difference between Associate Statistical Programmer vs Statistical Programmer?

AspectAssociate Statistical ProgrammerStatistical Programmer
Required CredentialsBachelor's degree in statistics, mathematics, or related field; some roles may require basic programming skillsBachelor's or master's degree; more experience in programming and statistical analysis
Work EnvironmentEntry-level, supporting senior programmers; often in clinical research or pharmaceutical companiesMore independent, handling complex analyses; similar industry settings
Employer & Industry UsageCommon in clinical trials, pharmaceutical, and biotech companiesUsed across similar industries, often as a step up from associate roles

The main difference between an Associate Statistical Programmer and a Statistical Programmer lies in experience and responsibility level. Associate roles are typically entry-level, focusing on supporting tasks under supervision, while Statistical Programmers handle more complex analyses independently. Both roles are vital in clinical research and biotech industries, with the associate position serving as a stepping stone to more advanced programming roles.

What are the key skills and qualifications needed to thrive as an Associate Statistical Programmer, and why are they important?

To thrive as an Associate Statistical Programmer, you need a solid background in statistics, programming (especially SAS or R), and familiarity with clinical trial data, typically supported by a degree in statistics, mathematics, or a related field. Proficiency with statistical software (such as SAS, R, or Python), CDISC standards, and data management tools is essential, and certifications in SAS programming can be advantageous. Attention to detail, strong problem-solving abilities, and effective communication skills help you collaborate with clinical teams and ensure data quality. These skills and qualities are vital for delivering accurate statistical analyses that support regulatory submissions and evidence-based decision-making in clinical research.
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Associate Statistical Programmer jobs near you

Associate Director, Statistical Programming

Sironax

Waltham, MA • On-site

Other

Posted 14 days ago

Job description

This role requires 3 days per week in Waltham, MA office


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.



About Sironax

Sironax is a global clinical-stage biotechnology company focused on developing innovative therapies for neurodegenerative, inflammatory, immunologic, and rare diseases. Driven by scientific excellence and a patient-centered mission, Sironax is expanding its global presence to transform treatment paradigms and improve outcomes for patients worldwide.


Equal Opportunity Employer

Sironax is an equal opportunity employer committed to diversity, equity, and inclusion. We welcome applicants from all backgrounds and are dedicated to creating a work environment where everyone feels valued and empowered.

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