ZipRecruiter

Log In

1

Senior Statistical Programmer Jobs in West Roxbury, MA

Treeline Biosciences

Head of Biometrics

Watertown, MA · On-site

$310K - $395K/yr

Manage the statistical programming function and ensure delivery of high-quality datasets and ... senior leadership team, delivering timely biometrics insights and presentation support for high ...

Treeline Biosciences

Head of Biometrics

Watertown, MA · On-site

$310K - $395K/yr

Manage the statistical programming function and ensure delivery of high-quality datasets and ... senior leadership team, delivering timely biometrics insights and presentation support for high ...

MIT Lincoln Laboratory

AL/ML Programmer

Lexington, MA · On-site

D. in electrical engineering, computer science, or another relevant discipline, or a Masters and ... senior leadership, and external partners. * Detail-oriented, able to multi-task, with the ability ...

MIT Lincoln Laboratory

AL/ML Programmer

Lexington, MA · On-site

D. in electrical engineering, computer science, or another relevant discipline, or a Masters and ... senior leadership, and external partners. * Detail-oriented, able to multi-task, with the ability ...

MIT Lincoln Laboratory

AL/ML Programmer

Lexington, MA · On-site

D. in electrical engineering, computer science, or another relevant discipline, or a Masters and ... senior leadership, and external partners. * Detail-oriented, able to multi-task, with the ability ...

Vrtx

Analytics CoE Senior Manager

Boston, MA

$144K - $216K/yr

The Senior Manager Director role is within HEOR's Analytics Center of Excellence (CoE), a ... This role will work closely with a team of statistical programmers to lead the execution of data ...

Zenas BioPharma

Senior Director, Biostatistics

Waltham, MA · 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 ...

previous page

Showing results 41-60

All JobsStatistical Programmer JobsSenior Statistical Programmer JobsSenior Statistical Programmer Jobs in West Roxbury, MA

Senior Statistical Programmer information

See West Roxbury, MA salary details

$84.5K

$131.4K

$171.6K

How much do senior statistical programmer jobs pay per year?

As of Aug 12, 2026, the average yearly pay for senior statistical programmer in West Roxbury, MA is $131,409.00, according to ZipRecruiter salary data. Most workers in this role earn between $109,600.00 and $151,600.00 per year, depending on experience, location, and employer.

What is a senior statistical programmer?

A Senior Statistical Programmer is responsible for developing, testing, and validating statistical programs used for clinical trial data analysis. They work primarily with statistical software like SAS to generate tables, listings, and figures (TLFs) for regulatory submissions and research studies. This role requires strong programming skills, knowledge of statistical methodologies, and an understanding of clinical trial processes. Senior Statistical Programmers also collaborate with statisticians, data managers, and regulatory teams to ensure data integrity and compliance with industry standards.

What are the key skills and qualifications needed to thrive as a senior statistical programmer, and why are they important?

To thrive as a Senior Statistical Programmer, a strong background in statistical analysis, programming (often in SAS and R), and a relevant degree such as in statistics, mathematics, or computer science is essential. Experience with regulatory submission standards (like CDISC SDTM/ADaM), clinical trial software, and certifications such as SAS Certified Advanced Programmer are highly valued. Outstanding attention to detail, problem-solving abilities, and effective communication skills help individuals excel in this collaborative and deadline-driven role. These skills are crucial for ensuring accurate data analysis, regulatory compliance, and successful teamwork in high-stakes research environments.

What are the typical responsibilities and team dynamics for a senior statistical programmer?

As a Senior Statistical Programmer, you will typically be responsible for designing, developing, and validating statistical programs for clinical trial data analysis and reporting. You’ll work closely with biostatisticians, data managers, and clinical project teams to ensure data quality and regulatory compliance, often contributing to the creation of submission datasets and study reports. The role usually involves both independent work and active collaboration, with seasoned programmers frequently mentoring junior staff and participating in process improvement initiatives. This team-oriented structure offers exposure to a variety of projects and stakeholders, making it a dynamic environment ideal for those who enjoy both analytical tasks and cross-functional teamwork.

What cities near West Roxbury, MA are hiring for Senior Statistical Programmer jobs? Cities near West Roxbury, MA with the most Senior Statistical Programmer job openings:
Senior Statistical Programmer jobs near you
Infographic showing various Senior Statistical Programmer job openings in West Roxbury, MA as of August 2026, with employment types broken down into 77% Full Time, and 23% Contract. Highlights an 61% In-person, and 39% Remote job distribution, with an average salary of $131,409 per year, or $63.2 per hour.

Senior Manager/Associate Director, Biostatistics

Beam Therapeutics

Cambridge, MA • On-site

Full-time

Re-posted 4 days ago

Job description

Position Overview:

Beam is seeking a Senior Manager/Associate Director, Biostatistics to support the statistical design, execution, analysis, and reporting of clinical trials across Beam's development programs. The ideal candidate will work closely with cross-functional study teams to provide statistical input, contribute to study-level strategy, and oversee CRO biometrics deliverables to support timely and high-quality trial execution.

Responsibilities:

  • Serve as the study-level statistician for one or more clinical studies and provide oversight of CRO biometrics deliverables.
  • Support clinical development teams in robust study design and execution, with a focus on efficient and data-driven decision making.
  • Contribute to clinical protocol development, including design evaluations and drafting of protocol statistical sections.
  • Lead or contribute to the development of statistical analysis plans, TLF shells, data specifications, data monitoring charters, and related study documents.
  • Generate or review TLFs and perform ad hoc analyses as needed.
  • Review CRF design, data management plans, and data transfer plans to ensure data collection supports trial objectives and planned statistical analyses.
  • Specify randomization schedules and support testing of their implementation as needed.
  • Contribute to the review, interpretation, and communication of clinical trial data.
  • Support the development of clinical study reports, regulatory documents, publications, manuscripts, posters, and abstracts.
  • Support regulatory submissions and responses to regulatory questions, as needed.
  • Provide statistical requirements and oversight to statistical programmers and external vendors.
  • Work collaboratively and communicate effectively with statistical programming, data management, clinical operations, clinical development, regulatory, and other cross-functional partners.

Qualifications:

  • Ph.D. in statistics, biostatistics, or a related field with a minimum of 4 years of relevant experience in the pharmaceutical or biotechnology industry.
  • Experience serving as a study-level statistician or statistical lead for clinical trials.
  • Strong knowledge of statistical methods and clinical trial design for rare disease and/or gene/cell therapy clinical trials is desirable.
  • Experience with statistical simulations, Bayesian methods, observational studies, and/or real-world data is desirable.
  • Experience supporting regulatory submissions, including NDA/BLA/MAA activities, is preferred.
  • Working knowledge of FDA and ICH regulations and guidelines; experience with gene/cell therapy programs is desirable.
  • Proficiency in SAS and/or R programming.
  • Strong knowledge of clinical data standards, including CDASH, SDTM, and ADaM.
  • Ability to work independently, manage priorities, and deliver high-quality work in a fast-paced environment.
  • Strong verbal and written communication skills.
  • Ability to build effective cross-functional relationships and work collaboratively with internal colleagues, CROs, and external vendors.

Apply