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Statistical Programmer Analyst Jobs in Boston, MA

Biogen

Sr. Analyst, Statistical Programming

Cambridge, MA · On-site

$95K - $130K/yr

About this role The Senior Analyst, Statistical Programming leads and oversees statistical programming activities both internally and externally through vendors in the application of data standards ...

Corrona

Biostatistical Data Programmer

Waltham, MA · On-site

Essential Functions: • Derives, compiles and formats data and structures for statistical analysis ... Preferred: • Experience programming in Java or Python. • Test-based/test-driven development ...

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Showing results 21-40

All JobsStatistical Programmer Analyst JobsStatistical Programmer Analyst Jobs in Boston, MA

Statistical Programmer Analyst information

See Boston, MA salary details

$67.5K

$109.7K

$166.1K

How much do statistical programmer analyst jobs pay per year?

As of Sep 5, 2026, the average yearly pay for statistical programmer analyst in Boston, MA is $109,709.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,600.00 and $137,800.00 per year, depending on experience, location, and employer.

What is a statistical programmer analyst?

Statistical Programmer Analysts are professionals who develop, test, and maintain statistical programs for analyzing data, typically in industries such as healthcare, pharmaceuticals, finance, and research. They work closely with statisticians and data managers to ensure data is accurately processed and reported, often using programming languages like SAS, R, or Python. Their responsibilities include creating analysis datasets, generating tables, listings, and figures, and ensuring compliance with regulatory requirements. Statistical Programmer Analysts play a key role in transforming raw data into meaningful insights that support decision-making and research outcomes.

What are the key skills and qualifications needed to thrive as a statistical programmer analyst?

To thrive as a Statistical Programmer Analyst, you need strong skills in statistical analysis, programming (especially in SAS, R, or Python), and a relevant degree in statistics, mathematics, or a related field. Familiarity with clinical trial data standards (like CDISC), data management systems, and regulatory submission requirements is often required, along with certifications in SAS or similar tools. Attention to detail, analytical thinking, and effective collaboration are critical soft skills for this role. These skills and qualities are vital to ensure accurate data analysis, regulatory compliance, and successful team-based project delivery in data-driven environments.

How do statistical programmer analysts typically collaborate with clinical research teams during a study?

Statistical Programmer Analysts work closely with clinical research teams, including biostatisticians, data managers, and clinical project managers, to ensure accurate analysis and reporting of clinical trial data. They are responsible for programming data sets, creating statistical tables, listings, and figures, and validating results to support regulatory submissions or publications. Effective communication and collaboration are essential, as they often attend regular team meetings to discuss requirements, troubleshoot data issues, and ensure timelines are met. This teamwork fosters a dynamic environment where analytical and technical expertise directly contribute to the success of clinical research projects.

What is the difference between Statistical Programmer Analyst vs Data Analyst?

AspectStatistical Programmer AnalystData Analyst
Required CredentialsBachelor's in Statistics, Computer Science, or related field; experience with SAS, R, or PythonBachelor's in Statistics, Data Science, or related field; proficiency in Excel, SQL, and visualization tools
Work EnvironmentPharmaceutical, clinical research, or healthcare industries; focus on programming and statistical analysisVarious industries including finance, marketing, healthcare; focus on data interpretation and reporting
Employer & Industry UsageCommon in clinical trials, biotech, pharma companiesWidely used across multiple sectors including business, finance, and healthcare

The main difference is that a Statistical Programmer Analyst primarily focuses on programming and analyzing clinical or research data using statistical software, while a Data Analyst often handles broader data interpretation and reporting across various industries. Both roles require similar technical skills but differ in industry focus and specific responsibilities.

What are popular job titles related to Statistical Programmer Analyst jobs in Boston, MA?

For Statistical Programmer Analyst jobs in Boston, MA, the most frequently searched job titles are:

What job categories do people searching Statistical Programmer Analyst jobs in Boston, MA look for?

The top searched job categories for Statistical Programmer Analyst jobs in Boston, MA are:

Statistical Programmer Analyst jobs near you
Infographic showing various Statistical Programmer Analyst job openings in Boston, MA as of August 2026, with employment types broken down into 87% Full Time, 8% Part Time, and 5% Contract. Highlights an 84% Physical, 6% Hybrid, and 10% Remote job distribution, with an average salary of $109,709 per year, or $52.7 per hour.

Manager, Statistical Programming

Rhythm Pharmaceuticals

Boston, MA • On-site

Full-time

Re-posted 6 days ago

Job description

Company Overview
Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases. We recognize the courage it takes for patients and their caregivers to begin their journey of advocacy to find the answers they need. Their courage inspires us to challenge convention, ask bold questions and seek answers for them. Every day, we strive for excellence through our willingness to adapt, learn, and our tenacity to overcome barriers, together.
Opportunity Overview
Rhythm is seeking a Manager, Statistical Programming to join our Biostatistics and Statistical Programming team. This role will provide statistical programming hands-on support across clinical studies, regulatory submissions, and cross-functional development activities. The successful candidate will be responsible for delivering high-quality, compliant analysis datasets, tables, listings, and figures; contributing to study-level and integrated submission deliverables; and partnering closely with Biostatistics, Data Management, Clinical Development, Medical Writing, Regulatory, and external vendors. Depending on level, the role may also include broader responsibility for study oversight, process improvement, standards development, vendor oversight, and mentoring programmers. The level will be determined based on the candidate’s experience, technical depth, and leadership capabilities.
Responsibilities and Duties
  • Lead or support statistical programming activities for assigned clinical studies, including development, validation, and quality control of analysis datasets, tables, listings, and figures for study reports, regulatory submissions, and internal decision-making.
  • Serve as a study lead programmer or programming representative, partnering closely with Biostatistics, Data Management, Clinical Development, Medical Writing, Regulatory, and external vendors to deliver high-quality results on time.
  • Develop, review, and maintain ADaM specifications, TLF shells, programming documentation, reusable macros, and study-level programming standards in alignment with company procedures and regulatory expectations.
  • Provide input into protocols, statistical analysis plans, CRF design and annotation, edit checks, SDTM specifications, integrated data review, and submission strategy to ensure traceability, consistency, and efficient downstream analysis.
  • Support regulatory submission readiness, including preparation and review of define.xml, reviewer guides, submission-ready datasets, and related documentation in compliance with CDISC and global regulatory requirements.
  • Identify programming risks, drive issue resolution, and recommend process improvements that enhance quality, scalability, efficiency, and inspection readiness across studies and programs.
  • Depending on level, mentor junior programmers, provide technical guidance, contribute to resource planning, oversee vendor deliverables, and help shape departmental standards, tools, and best practices.

Qualifications and Skills
  • MS or equivalent degree in Statistics, Biostatistics, Mathematics, Computer Science, or a related discipline; advanced degree preferred.
  • 5+ years relevant statistical programming experience in biotech, pharma, or CRO settings; vendor oversight experience preferred but not required.
  • Strong hands-on expertise in SAS programming, including Base SAS, SAS/STAT, SAS/GRAPH, SAS/SQL, SAS/ODS, and macro development; experience with R or other modern programming tools is a plus.
  • Deep knowledge of CDISC standards, including SDTM, ADaM, define.xml, reviewer guides, and electronic submission requirements in eCTD format.
  • Experience supporting study-level and integrated analyses, including ISS/ISE or other cross-study deliverables, with strong understanding of clinical trial reporting and regulatory submission processes.
  • Able to work independently, manage priorities, collaborate cross-functionally, and deliver high-quality work in a fast-paced environment.
  • For manager-level candidates, experience mentoring programmers, overseeing external vendors, and contributing to resource planning or process improvement is a plus.

This role is based out of our corporate office in Boston, Massachusetts. Rhythm operates in a hybrid-work model. Candidates applying must be willing and able to be in the Boston office in coordination with their department and business needs. This role may involve some travel.
The expected salary range for this position is $110,000 - $165,000. Actual pay will be determined based on experience, level, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and company performance. This role may be eligible for benefits and other compensation such as restricted stock units.
More about Rhythm
We are a dynamic and growing global team spanning more than a dozen countries. At Rhythm we are dedicated to transforming the lives of patients living with rare neuroendocrine diseases by rapidly advancing care and precision medicines that address the root cause.  Our team is passionate about expanding access to reach more patients and developing novel therapies for other rare neuroendocrine diseases, including congenital hyperinsulinism.
 
At Rhythm our core values are:
  • We are committed to advancing scientific understanding to improve patients’ lives
  • We are inspired to tackle tough challenges and have the courage to ask bold questions
  • We are eager to learn and adapt
  • We believe collaboration and ownership are foundational for our success
  • We value the unique contribution each individual brings to furthering our mission

Inherent in our core values is the commitment to act ethically and with integrity in all we do.
Rhythm is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service, or any other class protected by state or federal law. 
Headquartered in Boston, Rhythm is proud to have been named one of the Top Places to Work in Massachusetts.

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