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Associate Director Statistical Programming Jobs in Boston, MA

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 ...

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 ...

Head of Biometrics

Watertown, MA · On-site

$310K - $395K/yr

In your role as Head of Biometrics , you will be responsible for leading all biostatistics and statistical programming activities across Treeline's clinical and translational development programs.

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

Head of Biometrics

Watertown, MA · On-site

$310K - $395K/yr

Manage the statistical programming function and ensure delivery of high-quality datasets and ... agreement directed to the particular position or positions is in place at the start of the ...

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

Director of Biostatistics

Lynn, MA · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

Showing results 41-60

Associate Director Statistical Programming information

See Boston, MA salary details

$166.8K

$304.3K

$373.7K

How much do associate director statistical programming jobs pay per year?

As of Aug 10, 2026, the average yearly pay for associate director statistical programming in Boston, MA is $304,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $283,000.00 and $350,300.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an associate director statistical programming?

To thrive as an Associate Director Statistical Programming, you need expertise in statistical programming, clinical trial data standards, and a degree in statistics, mathematics, or a related field, often with several years of experience in the pharmaceutical or biotechnology industry. Proficiency in programming languages such as SAS and R, knowledge of CDISC standards (SDTM, ADaM), and familiarity with regulatory submission requirements are typically required. Strong leadership, project management, and communication skills are vital for guiding teams and collaborating with cross-functional partners. These skills and qualities ensure the delivery of high-quality, compliant statistical outputs that support clinical development and regulatory approval.

What does an associate director statistical programming do?

An Associate Director of Statistical Programming leads teams responsible for the design, development, and validation of statistical programs used in the analysis of clinical trial data. They oversee the creation of datasets, tables, listings, and figures that support regulatory submissions and scientific publications. In addition to technical expertise, this role involves managing timelines, ensuring compliance with regulatory standards, and collaborating with cross-functional teams such as biostatistics, data management, and clinical operations.

How does an associate director statistical programming typically collaborate with cross-functional teams in a pharmaceutical or biotech setting?

As an Associate Director of Statistical Programming, you will work closely with biostatisticians, clinical data managers, and regulatory affairs professionals to ensure that statistical analyses and data outputs meet project and regulatory requirements. You’ll often lead programming teams, coordinate timelines, and help translate statistical analysis plans into executable code. Regular meetings and clear communication are key, as you’ll be expected to provide technical guidance and ensure data integrity across multiple studies or programs. This role often requires balancing hands-on programming with strategic leadership and mentorship responsibilities.

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

AspectAssociate Director Statistical ProgrammingStatistical Programmer
Required CredentialsBachelor's or Master's in Biostatistics, Statistics, or related field; experience in clinical trial programmingBachelor's or Master's in similar fields; entry to mid-level experience
Work EnvironmentLeads teams, manages projects, collaborates with cross-functional teamsPerforms programming tasks, supports project teams, executes statistical analyses
Employer & Industry UsagePharmaceutical and biotech companies, clinical research organizationsPharmaceutical companies, CROs, biotech firms

The Associate Director Statistical Programming typically oversees programming teams and manages project deliverables, requiring leadership skills and extensive experience. In contrast, the Statistical Programmer focuses on executing programming tasks under supervision. Both roles are essential in clinical research, but the Associate Director holds more managerial responsibilities and strategic oversight.

What are popular job titles related to Associate Director Statistical Programming jobs in Boston, MA? For Associate Director Statistical Programming jobs in Boston, MA, the most frequently searched job titles are:
What job categories do people searching Associate Director Statistical Programming jobs in Boston, MA look for? The top searched job categories for Associate Director Statistical Programming jobs in Boston, MA are:
What cities near Boston, MA are hiring for Associate Director Statistical Programming jobs? Cities near Boston, MA with the most Associate Director Statistical Programming job openings:
Infographic showing various Associate Director Statistical Programming job openings in Boston, MA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 49% In-person, and 51% Hybrid job distribution, with an average salary of $304,336 per year, or $146.3 per hour.

Senior Manager Statistical Programming

Regeneron Pharmaceuticals

Cambridge, MA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 24 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

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 Senior Manager, Statistical Programming to join our Statistical Programming function, providing technical leadership across project teams within one or more therapeutic areas. In this role, you will drive high-quality programming deliverables from single studies through regulatory approval, product launch, and beyond, while collaborating with partnering functions, external service providers, and study teams. This position offers the opportunity to shape department strategy and mentor talent within a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

  • Location: Warren, NJ or Cambridge, MA
  • Work model/flexibility: hybrid-onsite

Discover your role:

  • Lead programming support across multiple studies, ensuring timely, high-quality deliverables
  • Coordinate programming documentation and specifications, following established standards
  • Champion company values through excellence, collaboration, and accountability
  • Communicate proactively with study and project teams to clarify requirements and guide programmers
  • Lead submission-ready programming deliverables for global regulatory authority filings
  • Drive department goals and serve as a subject matter expert on key topics
  • Guide the development of direct reports through goal-setting, coaching, and mentoring
  • Contribute to hiring by screening and interviewing programming candidates

This role might be for you if:

  • You bring advanced SAS skills honed in a clinical data environment, ideally across multiple therapeutic areas
  • You understand pharmaceutical clinical development, statistical concepts, and regulatory submission requirements
  • You collaborate naturally across global, interdisciplinary teams
  • You juggle multiple projects and priorities without losing sight of quality
  • You solve problems with initiative, creativity, and a self-starter mindset
  • You enjoy influencing, mentoring, and coaching others toward strong results
  • You lead with accountability and hold yourself to a high bar
  • You're energized by both hands-on programming work and people leadership

This role requires:

  • Advanced SAS programming expertise in a clinical data environment
  • Strong understanding of clinical trial principles and regulatory submission requirements
  • Proven ability to lead global, cross-functional teams
  • Experience managing multiple concurrent projects and priorities
  • Demonstrated mentoring or coaching experience with junior programmers
  • Education & experience: MS or BS in Statistics, Computer Science, Mathematics, Engineering, Life Science, or a related discipline, with 10+ years (12+ for BS) of programming experience - preferably in clinical trial data within biotechnology, pharmaceutical, or health-related industries, including some project and people management experience
  • Preferred/nice to haves: Knowledge of additional programming languages such as R or Python

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)

$150,500.00 - $245,500.00

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