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Director Statistical Programmer Jobs in Boston, MA

Servier

Senior Manager, Statistical Programming

Boston, MA · On-site

$151K - $172K/yr

Self-directed, technically strong, expert regarding statistical programming processes, management of statistical programmers at study level * Strong study management skills * Good negotiation and ...

Servier

Senior Manager, Statistical Programming

Boston, MA · On-site +1

$151K - $172K/yr

Self-directed, technically strong, expert regarding statistical programming processes, management of statistical programmers at study level * Strong study management skills * Good negotiation and ...

Treeline Biosciences

Director, Biostatistics

Watertown, MA · On-site

$226K - $257K/yr

Director of Biostatistics The Director of Biostatistics will lead the statistical strategy, design ... Analysis & Programming: Program, validate, and perform statistical analyses for trial data cuts ...

Treeline Biosciences

Director, Biostatistics

Watertown, MA · On-site

$226K - $257K/yr

Director of Biostatistics The Director of Biostatistics will lead the statistical strategy, design ... Analysis & Programming: Program, validate, and perform statistical analyses for trial data cuts ...

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All JobsStatistical Programmer JobsDirector Statistical Programmer JobsDirector Statistical Programmer Jobs in Boston, MA

Director Statistical Programmer information

See Boston, MA salary details

$91.8K

$160K

$270.5K

How much do director statistical programmer jobs pay per year?

As of Aug 21, 2026, the average yearly pay for director statistical programmer in Boston, MA is $160,018.00, according to ZipRecruiter salary data. Most workers in this role earn between $135,800.00 and $173,800.00 per year, depending on experience, location, and employer.

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

AspectDirector Statistical ProgrammerStatistical Programmer
Required credentialsBachelor's or Master's in Biostatistics, Statistics, or related field; often with experience in leadership rolesBachelor's or Master's in Biostatistics, Statistics, or related field; typically less managerial experience
Work environmentLeads teams, manages projects, collaborates with senior managementPerforms data analysis, programming, and reporting tasks under supervision
Employer and industry usagePharmaceutical, biotech companies, CROs, clinical research organizationsPharmaceutical, biotech companies, CROs, clinical research organizations

The main difference between a Director Statistical Programmer and a Statistical Programmer lies in their level of responsibility and leadership. The director oversees teams, manages projects, and interacts with senior management, while the statistical programmer focuses on executing data analysis and programming tasks. Both roles are essential in the clinical research industry, with the director position requiring more experience and strategic oversight.

What are the most commonly searched types of Statistical Programmer jobs in Boston, MA?

The most popular types of Statistical Programmer jobs in Boston, MA are:

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

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

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

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

What cities near Boston, MA are hiring for Director Statistical Programmer jobs?

Cities near Boston, MA with the most Director Statistical Programmer job openings:

Director Statistical Programmer jobs near you
Infographic showing various Director Statistical Programmer job openings in Boston, MA as of August 2026, with employment types broken down into 2% As Needed, 81% Full Time, 13% Part Time, 1% Temporary, and 3% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $160,018 per year, or $76.9 per hour.

Associate Director, Statistical Programming

Alkermes

Waltham, MA • On-site

$184K - $198K/yr

Full-time

Re-posted 25 days ago

Job description


The Associate Director of Statistical Programming, as a member of the Biostatistics & Statistical Programming Department, will contribute to Alkermes to achieve the goals of continuing growth in neuroscience. The Associate Director will combine technical and project management skills to lead programmers to develop and validate SAS programs to produce high quality deliverables for in-house and outsourced projects in CDISC compliance to meet regulatory requirements. In addition, this individual will support the automation and innovation within programming group to drive effective and efficient statistical programming.
Alkermes has recently adopted a hybrid working environment to support and meet the needs of employees and this role will operate in a flexible environment with 60% of time in the office and 40% from home. This position is eligible for the hybrid workplace model, requiring work to be completed onsite at our Waltham, MA office at least 3 days per week. This role is not eligible for fully remote work.
Responsibilities
  • Function as lead programmer to coordinate all activities related to study or project level statistical programming activities.
  • Design and develop programming specifications and SAS programs for producing and validating CDISC compliant datasets to support the generation of outputs for regulatory submission.
  • Produce and validate regulatory submission tables, figures and listings, support ad-hoc exploratory analysis in a timely fashion and of high quality
  • Design, develop, implement and maintain innovative statistical programming automation reporting tools to effectively support multiple projects.
  • Provide project management and technical guidance to ensure operational and technical excellence. Mentor junior level staff in programming practices, implementation of standards and project management.
  • Represent statistical programming in cross-functional teams. Work in close collaboration with other functions including biostatistics, clinical operations, data management and regulatory operations to define deliverables, develop timelines and ensure alignment of expectations
  • Work with IT to develop and maintain programming environment to ensure data security and efficient analysis and reporting

Qualifications
Basic Requirements:
  • Advanced degree strongly preferred (M.S. or Ph. D) with strong analytical skills
  • Minimum 8+ years experiences in pharmaceutical/biotech and/or CRO setting

Preferred Requirements:
  • Proven expert in SAS programming and analytical skills using BASE SAS, SAS/STAT, SAS/GRAPH and SAS MACROS etc.
  • Extensive CDISC SDTM and ADaM knowledge with significant experience writing ADaM specifications using robust and detailed instructions. Strong hands-on SAS programing skills for clinical trial reporting. Experience with electronic FDA submission.
  • Prefer proficiency in other data analysis programming languages, such as R and Python. Ability to learn new programming language quickly and be motivated to utilize them in the clinical development field.
  • Strong knowledge and understanding of GCP/ICH Guidelines for conducting clinical trials
  • Strong interpersonal, organizational, and multi-tasking skills
  • Excellent attention to detail and problem-solving skills
  • Good project management skills, CRO oversight skills, professional attitude, self-improvement mentality with positive attitude
  • Good written and oral presentation skills and ability to communicate effectively
  • Ability to think creatively and independently, and to form sound opinions and make sensible decisions in a dynamic environment
  • Neuroscience experience is a plus
  • SAS LSAF experience is a plus

The annual base salary for this position ranges from $184,071 to $198,796. In addition, this position is eligible for an annual performance pay bonus. Exact compensation may vary based on skills, training, knowledge, and experience. Alkermes offers a competitive benefits package. Additional details can be found on our careers website: www.alkermes.com/careers#working-here
#LI-HB1
About Us
Why join Team Alkermes?
Alkermes applies its decades of deep neuroscience expertise to develop medicines designed to help people living with complex and difficult-to-treat psychiatric and neurological disorders. A global biopharmaceutical company, headquartered in Ireland with U.S. locations in Massachusetts and Ohio, we seek to make a meaningful difference in the way people manage their diseases. We have a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia, bipolar I disorder and narcolepsy, and a pipeline of clinical and preclinical candidates in development for various psychiatric and neurological disorders.
We are proud to have been recognized as an employer of choice by many national organizations. In 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts' Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine.
Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any qualified applicant or employee because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender expression and identity, disability, genetic information, veteran status, military status, application for military service or any other characteristic protected by local, state or federal law. Alkermes also complies with all work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Alkermes is an E-Verify employer.

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