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Senior Statistical Programmer Jobs in West Roxbury, MA

As a senior statistical leader and cross‑functional partner, this role leads statistical ... Management, Statistical Programming, Translational Medicine, Program Management, and other ...

Data Scientist I

Somerville, MA · On-site

$140 - $170/hr

... senior statistical and clinical partners. You will learn to reason carefully under uncertainty ... Building with others You will work closely with clinical, statistical, engineering, and product ...

Senior Manager, Biostatistics

Boston, MA · On-site

$119K - $157K/yr

The Senior Manager, Biostatistics has sufficient experience working as a statistician in the ... Competent statistical programmer (SAS and R) * Knowledge of key technical and regulatory ...

Showing results 21-40

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:
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.

Manager Statistical Programming

Regeneron Pharmaceuticals

Cambridge, MA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 4 days ago


Regeneron rating

8.7

Company rating: 8.7 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

14th of 86 rated pharmaceutical


Job description

ion

Build our future together:

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Statistical Programming to join our Statistical Programming team, supporting a study team across our clinical portfolio. In this role, you will lead programming deliverables from a single study through regulatory approval, product launch, and annual reports, while collaborating with study teams, CROs, and cross-functional colleagues to ensure timely, high-quality analysis and reporting.

This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

  • Location: Warren, NJ or Cambridge, MA

  • Work model/flexibility: Onsite

Discover your role:

  • Develop expertise within a therapeutic area or standard tool, working independently to coordinate and oversee project deliverables

  • Lead the development and quality control of tables, listings, and graphs in support of analysis requirements

  • Manage programming effort, tracking progress and completion of deliverables, including complex ad hoc requests

  • Serve as programming representative on a multidisciplinary study team, ensuring timely support through regulatory approval and launch

  • Partner with management to determine resource requirements for your therapeutic area or department

  • Contribute to hiring by reviewing resumes and screening candidates for contractor and permanent roles

  • Provide feedback to management on team members' contributions to support performance evaluations and goal-setting

  • Advise direct reports on procedures for data, records, and information retention

This role might be for you if you:

  • Enjoy working with minimal supervision and taking ownership of complex deliverables

  • Communicate clearly with cross-functional, multidisciplinary teams

  • Think analytically and stay organized when managing multiple priorities and timelines

  • Take initiative in developing deep expertise within a specialized area

  • Bring a collaborative mindset to hiring, feedback, and team development

  • Adapt easily to shifting priorities, including last-minute requests from senior leadership

  • Approach quality and documentation with rigor in a regulated environment

This role requires:

  • Master's degree with 8-10 years of relevant work experience (or a Master's degree in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related discipline with 5+ years of relevant programming experience, including some project and people management experience)

  • Proven experience leading programming deliverables within a clinical study team

  • Experience providing input on hiring, feedback, and performance evaluation

  • Strong organizational and documentation skills within a regulated environment

Nice to haves:

  • SAS Certification

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.


Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed onsite. Please speak with your recruiter and hiring manager for more information about onsite expectations for your role and location.


As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.


For jobs in Canada: this posting is for an existing position.


Salary Range (annually)

$128,600.00 - $210,000.00

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