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Director Statistical Programming Jobs in Medford, 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 ...

Role Summary The Senior Director, Biostatistics provides strategic, technical, and operational ... Management, Statistical Programming, Translational Medicine, Program Management, and other ...

The Executive Director will serve as the project-level biostatistician, providing expertise in the ... SAS analysis programming skills. * Experience with statistical software and graphics packages.

The Executive Director will serve as the project-level biostatistician, providing expertise in the ... SAS analysis programming skills. * Experience with statistical software and graphics packages.

Director, Data Management

Waltham, MA · On-site

$205K - $230K/yr

The Director partners closely with cross-functional stakeholders, including Clinical Operations, Biostatistics, Statistical Programming, Medical Monitoring, Clinical Systems, Quality Assurance, and ...

The Senior Director of Biostatistics is accountable for providing statistical leadership and ... Proficiency in SAS programming and other statistical software tools. * Ability to manage people and ...

Showing results 41-60

Director Statistical Programming information

See Medford, MA salary details

$160K

$291.9K

$358.5K

How much do director statistical programming jobs pay per year?

As of Sep 2, 2026, the average yearly pay for director statistical programming in Medford, MA is $291,926.00, according to ZipRecruiter salary data. Most workers in this role earn between $271,500.00 and $336,100.00 per year, depending on experience, location, and employer.

What is a director statistical programming?

The job of a director of statistical programming oversees the development and implementation of SAS programs to produce statistical analysis datasets. In this career, your responsibilities include managing the team that generates tables and graphs using the SAS programs for applications such as clinical studies. Other duties include participating in the planning and review of statistical analysis and studying reports, abstracts, and manuscripts as required. You collaborate with project leads to contribute to department operations and standards, such as CDISC for clinical research.

What does a director statistical programming do?

A Director of Statistical Programming oversees teams responsible for the programming and analysis of clinical trial data, ensuring the accuracy and integrity of statistical outputs. They set departmental strategies, manage resources, and ensure compliance with regulatory requirements and industry standards. This role also involves collaborating with other departments, such as biostatistics and clinical operations, to support the successful delivery of statistical analyses for drug development and regulatory submissions. They play a key leadership role in mentoring staff and advancing programming processes and technologies.

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

To thrive as a Director of Statistical Programming, you need advanced expertise in statistical analysis, programming languages such as SAS or R, and a strong background in clinical trial data, typically supported by a degree in statistics, mathematics, or a related field. Familiarity with regulatory submission processes, CDISC standards, and project management tools is essential, as are relevant certifications like SAS Certified Professional. Leadership, effective communication, and strategic thinking are key soft skills for managing teams and collaborating across departments. These skills ensure high-quality data outputs, regulatory compliance, and successful execution of complex clinical development projects.

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

A Director of Statistical Programming regularly works with biostatistics, clinical data management, regulatory affairs, and medical writing teams to ensure that statistical deliverables meet project timelines and regulatory requirements. They coordinate programming efforts across multiple studies, provide leadership and mentorship to programming staff, and help resolve technical or resource-related challenges. Effective collaboration is essential to streamline workflows, maintain data integrity, and ensure clear communication of statistical results within the organization.

What are popular job titles related to Director Statistical Programming jobs in Medford, MA?

For Director Statistical Programming jobs in Medford, MA, the most frequently searched job titles are:

What job categories do people searching Director Statistical Programming jobs in Medford, MA look for?

The top searched job categories for Director Statistical Programming jobs in Medford, MA are:

What cities near Medford, MA are hiring for Director Statistical Programming jobs?

Cities near Medford, MA with the most Director Statistical Programming job openings:

Infographic showing various Director Statistical Programming job openings in Medford, MA as of August 2026, with employment types broken down into 89% Full Time, 8% Part Time, and 3% Contract. Highlights an 79% In-person, 11% Hybrid, and 10% Remote job distribution, with an average salary of $291,926 per year, or $140.3 per hour.

Senior Programmer, EDC Systems

CSL Plasma Inc.

Waltham, MA • On-site

$120 - $150/hr

Other

Posted 12 days ago


CSL Plasma rating

5.9

Company rating: 5.9 out of 10

Based on 359 frontline employees who took The Breakroom Quiz

766th of 898 rated healthcare providers


Job description

Position Purpose:

The Senior EDC Programmer focuses on governance, review, and validation of deliverables to ensure alignment with CSL standards, regulatory requirements, and industry best practices. The incumbent applies strong expertise in leading and overseeing set-up and maintenance of Clinical Data Management Systems in addition to providing technical support. This individual supports cross-functional teams such as Statistics, Data Management and Standards by overseeing and ensuring the quality of clinical data build and programming activities across in-house, hybrid, and vendor-supported studies. The role will contribute to shaping future-state data capabilities by supporting initiatives around scalable data platforms and AI-driven automation, enabling more efficient and intelligent use of clinical data.

Reporting Relationships:

This role reports to the Director, Statistical Programming Lead

Work Environment:

*** On site / Hybrid at CSL

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Pay

Benefits

Hours and flexibility

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About CSL Plasma

Sourced by ZipRecruiter

Supported by parent company CSL Behring, the global leader in plasma protein biotherapeutics, CSL Plasma has more than 300 plasma collection centers globally. CSL Plasma also has a state-of-the-art testing laboratory that features some of the most advanced technology, instrumentation and automation in the field; two logistics centers, one in Dallas and one in Indianapolis. Our corporate headquarters is in Boca Raton, Florida. Our U.S. plasma collection centers are committed to the highest standards of quality and safety. When you donate, you give a valuable gift to those who require plasma-derived therapies to live healthier lives. The CSL Group has a combined heritage of outstanding contribution to medicine and human health with more than 100 years' experience in the development and manufacture of vaccines and plasma protein biotherapies. With major facilities in Australia, Germany, Switzerland and the US, CSL has over 30,000 employees working in 100 countries.

Industry

Medical equipment and supplies manufacturing and biotechnology research and development

Company size

10,000+ Employees

Headquarters location

Boca Raton, FL, US

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