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Manager Statistical Programming Jobs in Massachusetts

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Manager Statistical Programming information

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$92.3K

$160.9K

$271.9K

How much do manager statistical programming jobs pay per year?

As of Jul 13, 2026, the average yearly pay for manager statistical programming in Massachusetts is $160,861.00, according to ZipRecruiter salary data. Most workers in this role earn between $136,500.00 and $174,700.00 per year, depending on experience, location, and employer.

What is a Manager Statistical Programming job?

A Manager Statistical Programming oversees a team of statistical programmers who support clinical trials and research by developing, validating, and maintaining statistical programs. They ensure compliance with regulatory requirements, manage project timelines, and collaborate with statisticians, data managers, and other stakeholders. This role requires strong programming skills in SAS or other statistical software, leadership abilities, and expertise in clinical data standards such as CDISC.

What are the typical daily responsibilities of a Manager Statistical Programming?

As a Manager Statistical Programming, your daily responsibilities usually include overseeing a team of statistical programmers, coordinating the development and validation of statistical programs for clinical trial data analysis, and ensuring deliverables meet regulatory and company quality standards. You will often interact with biostatisticians, data managers, and clinical teams to align programming outputs with study goals. Additionally, you may review project timelines, allocate resources, mentor junior programmers, and contribute to process improvement initiatives. This multifaceted role requires balancing technical oversight with leadership and interdepartmental communication.

What are the key skills and qualifications needed to thrive in the Manager Statistical Programming position, and why are they important?

To excel as a Manager Statistical Programming, you need a solid background in statistics, programming (such as SAS, R, or Python), and experience with clinical trial data management, often supported by a degree in statistics, mathematics, or a related field. Familiarity with regulatory guidelines (e.g., FDA, ICH), data standards such as CDISC, and certifications in relevant programming languages or clinical data processes are highly beneficial. Strong leadership, project management, and effective communication skills are essential for guiding teams and collaborating with cross-functional departments. These skills enable the manager to deliver high-quality statistical programming deliverables, ensure regulatory compliance, and drive team performance in a deadline-driven environment.

What are the most commonly searched types of Statistical Programming jobs in Massachusetts? The most popular types of Statistical Programming jobs in Massachusetts are:
What are popular job titles related to Manager Statistical Programming jobs in Massachusetts? For Manager Statistical Programming jobs in Massachusetts, the most frequently searched job titles are:
What job categories do people searching Manager Statistical Programming jobs in Massachusetts look for? The top searched job categories for Manager Statistical Programming jobs in Massachusetts are:
What cities in Massachusetts are hiring for Manager Statistical Programming jobs? Cities in Massachusetts with the most Manager Statistical Programming job openings:
Manager Statistical Programming jobs near you
Associate Director, Statistical Programming

Associate Director, Statistical Programming

Verastem

Needham, MA • On-site, Remote

$165K - $190K/yr

Full-time

Posted 28 days ago

Job description

Job Title: Associate Director, Statistical Programming


Job Duties:


  • Lead design and development SAS programs and the programming specifications for producing and validating CDISC ADaM datasets to support the generation of tables, figures and listings for clinical study report(s), FDA submission(s), and medical congress abstracts/posters/presentations;
  • Responsible for internal statistical programming deliveries across multiple clinical studies, as well as implementing process improvements and department initiatives;
  • Identify areas within clinical development functions where statistical programming tools and applications can enhance processes;
  • Perform quality control checks of advanced SAS code and output produced by other statistical programmers;
  • Work closely with clinical operations, data management and statisticians to develop infrastructure for timely and quality reporting of clinical trials to support regulatory requirements, and product launch activities;
  • Proactively identify issues and recommend solutions to optimize preparation, execution, reporting, and documentation of statistical programming activities;
  • Provide project management and technical guidance to ensure operational and technical excellence;
  • Liaise with vendors as needed to facilitate electronic data transfers and statistical programming support.

Requirements: Requirements include a Bachelor's or equivalent in Regulatory Affairs, Statistics, Computer Science or related field plus nine years of work experience in the job offered or related fields of clinical data and statistical programming in pharmaceutical or biotech industries; or in the alternative, a Master's degree or equivalent in Regulatory Affairs, Statistics, Computer Science or related field plus seven years of work experience in the job offered or related fields of clinical data and statistical programming in pharmaceutical or biotech industries.

Special Requirements:

If qualifying with bachelor's degree, must have the following:

  • 9 years of experience with SAS programing;
  • 9 years of experience using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS;
  • 7 years of experience with CDISC SDTM and ADaM;
  • 7 years of experience with electronic FDA submission; and
  • 9 years of experience working in a clinical trial setting.

If qualifying with Master's degree, must have the following:

  • 7 years of experience with SAS programing;
  • 7 years of experience using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS;
  • 5 years of experience with CDISC SDTM and ADaM;
  • 5 years of experience with electronic FDA submission; and
  • 7 years of experience working in a clinical trial setting.


Work Location: Needham, MA

May work remotely from anywhere in U.S.

Multiple positions available. Applicants must have unrestricted authorization to work in the United States.

Salary: $165,000.00 - $190,000.00/year. 40 hours/wk full-time.

If interested and qualified for this position, please apply below.

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