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Sr Statistical Programmer Jobs in Boston, MA (NOW HIRING)

Cytel

Senior Statistical Programmer FSP

Cambridge, MA · On-site +1

As a Senior Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are ...

Servier

Senior Manager, Statistical Programming

Boston, MA · On-site

$151K - $172K/yr

Role Summary The Sr Manager, Statistical Programming is responsible for the development of statistical programming on the study level by performing hands-on programming or oversight of outsourced ...

Servier

Senior Manager, Statistical Programming

Boston, MA · On-site +1

$151K - $172K/yr

Role Summary The Sr Manager, Statistical Programming is responsible for the development of statistical programming on the study level by performing hands-on programming or oversight of outsourced ...

Vrtx

Principal Statistical Programmer

Boston, MA · Remote

$149K - $223K/yr

The Principal Statistical Programmer works with management to delegate tasks appropriately, track ... Senior Management levels * Creates all files, documents, and analyses necessary to support an ...

Cytel

Senior R Statistical Programmer

Cambridge, MA · On-site +1

The R Technical Solutions Programmer is responsible for implementing the vision for data and analysis infrastructure platforms and other technical solutions to support the data flow from data ...

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Sr Statistical Programmer information

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How much do sr statistical programmer jobs pay per year?

As of Aug 22, 2026, the average yearly pay for sr statistical programmer in Boston, MA is $139,371.00, according to ZipRecruiter salary data. Most workers in this role earn between $116,200.00 and $160,800.00 per year, depending on experience, location, and employer.

What is a Sr Statistical Programmer?

Sr Statistical Programmers are experienced professionals who specialize in managing and analyzing complex data sets, typically in the clinical research and pharmaceutical industries. They use statistical software like SAS or R to develop and validate programs that support clinical trials, regulatory submissions, and data reporting. Their responsibilities often include ensuring data quality, creating analysis datasets, generating tables, listings, and figures, and collaborating with statisticians and data managers. Senior-level programmers also mentor junior staff and may oversee project timelines and deliverables. Their expertise is essential for turning raw clinical data into meaningful results that support drug development and regulatory decision-making.

What are the key skills and qualifications needed to thrive as a Sr Statistical Programmer?

To thrive as a Sr Statistical Programmer, you need strong expertise in statistical programming languages like SAS or R, experience with clinical trial data, and a relevant degree in statistics, mathematics, or a related field. Proficiency with CDISC standards (SDTM, ADaM), data management systems, and regulatory submission tools is typically required. Excellent problem-solving, attention to detail, and effective communication are crucial soft skills for collaborating with cross-functional teams and ensuring high data quality. These skills and qualifications are essential for accurate analyses, regulatory compliance, and successful delivery of clinical research projects.

How does a Sr Statistical Programmer typically collaborate with biostatisticians and clinical teams during a clinical trial project?

As a Sr Statistical Programmer, you will work closely with biostatisticians to translate statistical analysis plans into efficient programming code, often using SAS or R. You’ll also regularly interact with clinical data managers and project teams to clarify data requirements, resolve data discrepancies, and ensure the accuracy of deliverables. Effective communication and proactive problem-solving are key, as you may be responsible for leading programming efforts, mentoring junior programmers, and ensuring that all outputs meet regulatory and project timelines. This collaborative environment helps ensure the integrity and reproducibility of clinical trial results.

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Sr Statistical Programmer jobs near you
Infographic showing various Sr Statistical Programmer job openings in Boston, MA as of August 2026, with employment types broken down into 71% Full Time, and 29% Contract. Highlights an 100% In-person job distribution, with an average salary of $139,371 per year, or $67 per hour.

Senior Statistical Programmer FSP

Cytel

Cambridge, MA • On-site, Remote

Full-time

Re-posted yesterday

Job description


Sponsor-dedicated:
Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Senior Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.
Position Overview:
As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote.
Our values
  • We believe in applying scientific rigor to reveal the full promise inherent in data.
  • We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery.
  • We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities.
  • We prize innovation and seek intelligent solutions using leading-edge technology.

Responsibilities
How you will contribute:
  • Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming
  • Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs)
  • Production and QC / validation programming
  • Generating complex ad-hoc reports utilizing raw data
  • Applying strong understanding/experience of Efficacy analysis
  • Creating and reviewing submission documents and eCRTs
  • Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries
  • Performing lead duties when called upon
  • Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.
  • Being adaptable and flexible when priorities change

Qualifications
Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have:
  • Bachelor's degree in one of the following fields Statistics, Computer Science, Mathematics, etc.
  • At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor's degree or equivalent. At least 6 years of related experience with a master's degree or above.
  • Study lead experience, preferably juggling multiple projects simultaneously preferred.
  • Strong SAS data manipulation, analysis and reporting skills.
  • Solid experience implementing the latest CDISC SDTM / ADaM standards.
  • Strong QC / validation skills.
  • Good ad-hoc reporting skills.
  • Proficiency in Efficacy analysis.
  • Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials' data.
  • Submissions experience utilizing define.xml and other submission documents.
  • Experience supporting immunology, respiratory or oncology studies would be a plus.
  • Excellent analytical & troubleshooting skills.
  • Ability to provide quality output and deliverables, in adherence with challenging timelines.
  • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.

Apply