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Director Statistical Programmer Jobs (NOW HIRING)

AstraZeneca

Director, Statistical Programming

Waltham, MA · On-site

$168K - $253K/yr

We are now offering an exciting opportunity for a dedicated and highly motivated individual to join us in the role as Statistical Programming Director, providing strategic programming leadership and ...

AstraZeneca

Director, Statistical Programming

Waltham, MA · On-site

$168K - $253K/yr

We are now offering an exciting opportunity for a dedicated and highly motivated individual to join us in the role as Statistical Programming Director, providing strategic programming leadership and ...

AstraZeneca

Director, Statistical Programming

Waltham, MA · On-site

$253K/yr

We are now offering an exciting opportunity for a dedicated and highly motivated individual to join us in the role as Statistical Programming Director, providing strategic programming leadershipand ...

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Director Statistical Programmer information

See salary details

$84.5K

$147.3K

$249K

How much do director statistical programmer jobs pay per year?

As of Aug 5, 2026, the average yearly pay for director statistical programmer in the United States is $147,292.00, according to ZipRecruiter salary data. Most workers in this role earn between $125,000.00 and $160,000.00 per year, depending on experience, location, and employer.

How much do statistical programmers make in the US?

Statistical programmers in the US typically earn between $80,000 and $130,000 annually, depending on experience, education, and location. Senior roles or those with specialized skills in programming languages like SAS or R can command higher salaries, often exceeding $140,000. Compensation also varies based on industry and company size.

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.

More about Director Statistical Programmer jobs
What cities are hiring for Director Statistical Programmer jobs? Cities with the most Director Statistical Programmer job openings:
What are the most commonly searched types of Statistical Programmer jobs? The most popular types of Statistical Programmer jobs are:
What states have the most Director Statistical Programmer jobs? States with the most job openings for Director Statistical Programmer jobs include:
What job categories do people searching Director Statistical Programmer jobs look for? The top searched job categories for Director Statistical Programmer jobs are:
Director Statistical Programmer jobs near you
Infographic showing various Director Statistical Programmer job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 84% Full Time, 12% Part Time, 1% Temporary, and 2% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $147,292 per year, or $70.8 per hour.

Associate Director, Statistical Programming

Servier

Boston, MA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 22 days ago

Job description

About Servier
Servier in the U.S. is a Boston-based, commercial-stage biopharmaceutical company launched by Servier Group in 2018. As a privately held organization, Servier is uniquely positioned to advance cutting-edge science, tackle underserved therapeutic areas and make patients the focus of every strategic decision.
Job Description
Role Summary
The Associate Director, Statistical Programming leads statistical programming activities for multiple studies, an asset or an indication by performing hands-on programming or oversight of outsourced deliverables. This individual will ensure that the statistical programming processes and deliverables are aligned with regulatory requirements and internal procedures. The role will interact closely with the study statisticians and study team regarding statistical programming aspects.
Primary Responsibilities
  • Manage statistical programming deliverables on one or more assets or indications by managing study leads and oversee study activities and vendor oversight.
  • Oversee development and quality control or oversight plan of analysis datasets and outputs for individual study as well as integrated analyses.
  • Ensure study leads deliver high quality, traceability, reproducibility of study outputs and timeliness of statistical programming deliverables to meet expectations and regulatory requirements.
  • Mentor statistical programmers with regards to programming activities and project management.
  • Independently implement routine and non-standard analysis algorithms for assigned projects or studies.
  • Collaborate with statisticians, local and CRO programmers to define and implement analysis requirements and perform sponsor oversight regarding data and analysis.
  • Ensure an efficient collaboration with all members of the clinical study team.
  • Ensure the statistical programming systems, processes and deliverables are aligned with the relevant regulatory requirements, for instance:
    • Clinical study reporting, e.g. ICH E3
    • Electronic records handling, e.g. Chapter 21 of the US Code of Federal Regulation - Part 11
    • Electronic submission of clinical data to agencies, e.g. e-CTD guidance and CDISC SDTM and ADaM standards.
    • Ensure that the datasets (SDTMs and ADaMs) are CDISC compliant.
  • Support on the design of new statistical programming processes or optimization of existing ones to reach the best productivity, to ensure the best quality of the statistical outputs, and to reach the best customer satisfaction (internally and externally) with flexibility, reliability and responsiveness.
  • Work with the portfolio programming lead to create forecasts for different studies and resource requirements.

Other responsibilities
  • Participate in working groups (either inter department or cross functional).
  • Participate in the preparation of audit/inspection and could interact with auditors/inspectors.
  • Contribute to the establishment and maintenance of common formats and templates for key Programming documentation (e.g., standard CRF pages, Tables, Figures and Listings).
  • Plan and track project activities, timelines across projects. Provide justification for planned resource needs. Seek to optimize resource utilization and capacity. Accurate plans, well-managed projects, capacity to apply extra resources in urgent situation.

Education and Required Skills
  • Masters in Statistics, Engineering or relevant field required with a minimum of 8 years of experience in statistical programming or biostatistics in the Pharmaceutical/Biotechnology industry in clinical development desirable
  • Experience with statistical programming in Oncology desirable
  • Proficient in SAS
  • Good knowledge of CDISC ADaM and SDTM
  • Strong knowledge of relevant regulatory and data submission guidelines
  • Strong understanding of drug development, including knowledge of interfaces and interdependencies with other functions
  • Self-directed, technically strong, expert regarding statistical programming processes, management of statistical programmers at study level
  • Strong study management skills
  • Good negotiation and issue resolution skills
  • Ability to organize team work and prioritize and balance concurrent tasks and responsibilities.
  • Excellent time management skills
  • Ability to educate internal and external interfaces (CROs and contractors) on the statistical programming processes, and the underlying regulatory requirements

Travel and Location
  • Some domestic and international travel required
  • On-site in Boston (recommended 2-3 days hybrid) or 100% remote with occasional travel to Boston

Servier's Commitment
Servier is committed to modeling diversity, equity, and inclusion within the industry. We are dedicated to fostering an environment that maintains equitable treatment for all and we welcome applicants who are passionate, committed, and innovative individuals. We encourage candidates to apply to our open roles as we are always willing to consider experiences and skills beyond what is listed in the job description.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Salary Range
The salary range for this role is $165,000-$200,000. An employee's pay position within the salary range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, geographic location, performance, and business or organizational needs. We may ultimately pay more or less than the posted range, and the range may be modified in the future. Employees in this position are also eligible for Short-Term and Long-Term incentive programs. Servier also offers a competitive and comprehensive benefits package that includes benefits such as medical, dental, vision, flexible time off (Servier provides unlimited sick time and flex time, and does not accrue time off), 401(k), life and disability insurance, recognition programs among other great benefits (all benefits are subject to eligibility requirements). For more information on our benefits, please visit this link.

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