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Associate Sas Programmer Jobs in Massachusetts (NOW HIRING)

Associate Director, Biostatistics

Woburn, MA ยท On-site

$194 - $251/hr

Summary of The Associate Director, Biostatistics, provides statistical support in one or more ... Good knowledge of statistical programming languages (including SAS). * Knowledge of SDTM/ ADaM.

New

... engineering, environmental science or a related field. A GPA of 3.5 or higher is highly desirable ... Proficiency in Excel is required; experience with MS SQL Server, R, Python, Stata, SAS, Tableau ...

Collaborates with statistical programming and other functions to ensure timely delivery of TFLs ... In-depth competence with SAS and R statistical software * In-depth understanding of advanced ...

2027 Summer Associate (Intern)

Boston, MA ยท On-site

$16.25 - $21.75/hr

... Stata,SAS,Python, or Snowflake. * Interact with senior staff,experts,and clients ... Experience with statistical, econometric and programming tools such as Excel, Stata, R, Python ...

2027 Summer Associate (Intern)

Boston, MA ยท On-site

$16.25 - $21.75/hr

... Stata,SAS,Python, or Snowflake. * Interact with senior staff,experts,and clients ... Experience with statistical, econometric and programming tools such as Excel, Stata, R, Python ...

$26.87 - $33.59/hr

... SAS, SPSS, or S-Plus. 4. Experience teaching statistics and statistical programming. Duties and Responsibilities: The duties and responsibilities listed below are intended to describe the general ...

... SAS, SPSS, or S-Plus. 4. Experience teaching statistics and statistical programming. Duties and Responsibilities: The duties and responsibilities listed below are intended to describe the general ...

... SAS, SPSS, or S-Plus. 4. Experience teaching statistics and statistical programming. Duties and Responsibilities: The duties and responsibilities listed below are intended to describe the general ...

Showing results 41-60

Associate Sas Programmer information

See Massachusetts salary details

$16

$53

$86

How much do associate sas programmer jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for associate sas programmer in Massachusetts is $53.52, according to ZipRecruiter salary data. Most workers in this role earn between $37.55 and $67.21 per hour, depending on experience, location, and employer.

What is an Associate SAS Programmer?

An Associate SAS Programmer is an entry-level professional who specializes in using SAS (Statistical Analysis System) software to manage, analyze, and report data. They typically assist more senior programmers and statisticians in preparing datasets, writing code, and generating statistical reports, often within industries such as healthcare, finance, or research. This role requires a good understanding of SAS programming language, attention to detail, and the ability to follow standard operating procedures. Associate SAS Programmers often work as part of a larger data or analytics team, supporting projects by ensuring data integrity and accurate analyses.

What are the key skills and qualifications needed to thrive as an Associate SAS Programmer?

To thrive as an Associate SAS Programmer, you need a solid understanding of statistical analysis, data management, and proficiency in SAS programming, often supported by a degree in statistics, computer science, or a related field. Familiarity with SAS software, data visualization tools, and knowledge of regulatory requirements or CDISC standards are typically expected, and SAS certification can be an advantage. Attention to detail, problem-solving ability, and effective communication are key soft skills for this role. These skills are crucial for ensuring accurate data analysis, efficient workflow, and clear reporting in data-driven environments such as clinical research or business analytics.

What are the typical responsibilities of an Associate SAS Programmer?

As an Associate SAS Programmer in clinical research, you will primarily be responsible for writing and validating SAS programs to analyze clinical trial data, generate tables, listings, and figures, and ensure data integrity and compliance with regulatory standards. Your daily tasks may also include collaborating closely with statisticians, data managers, and senior programmers to review requirements and resolve data issues. This role often involves learning industry best practices and becoming familiar with CDISC standards, offering a strong foundation for career advancement in clinical data programming.
What are the most commonly searched types of Sas Programmer jobs in Massachusetts? The most popular types of Sas Programmer jobs in Massachusetts are:
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What cities in Massachusetts are hiring for Associate Sas Programmer jobs? Cities in Massachusetts with the most Associate Sas Programmer job openings:
Infographic showing various Associate Sas Programmer job openings in Massachusetts as of August 2026, with employment types broken down into 1% As Needed, 73% Full Time, 24% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $111,319 per year, or $53.5 per hour.

Associate Director, Biostatistics

Clinical Dynamix, Inc.

Burlington, MA โ€ข On-site

Full-time

Re-posted 13 days ago


Job description

Associate Director, Biostatistics Job Description:

Position Summary

The Associate Director, Biostatistics is responsible for partnering with clinical, regulatory, data

management and statistical programming teams to deliver robust statistical methodologies that

advance clinical program objectives and ensure compliance with industry standards. This

individual will contribute to the success of the team and organization by delivering on role-

specific responsibilities while upholding our core working behaviors of Trust and Respect,

Communication and Feedback, Accountability and Reliability, Objectivity, and Team Balance and

Enablement.

Key Responsibilities

• Serve as the lead statistician for clinical trials, contributing to efficient study design and

rigorous data analysis.

• Provide high-quality statistical support across clinical programs, ensuring scientific

robustness and alignment with development goals.

• Design and refine clinical trial methodologies; author study synopses and protocols.

• Collaborate with data management on CRF design and database quality to ensure reliable

datasets.

• Develop statistical analysis plans and ensure clear, transparent documentation.

• Guide and mentor statistical programmers in creating SDTM/ADaM specifications, datasets,

and statistical outputs.

• Review and approve statistical deliverables to ensure consistency, accuracy, and regulatory

readiness.

• Interpret study results and contribute to clinical reports, presentations, publications, and

regulatory documentation.

• Author statistical content for regulatory submissions and support interactions with global

health authorities.

• Monitor timelines, deliverables, and support resource planning to keep programs on track.

• Participate in vendor selection and provide oversight to ensure high-quality, timely

statistical outputs.

• Contribute to the development and evolution of Biostatistics processes, standards, and best

practices at Company.

• Communicate proactively, collaborate effectively, and maintain a solutions-oriented

approach in a dynamic, fast-paced environment.

• Demonstrate ownership, accountability, and a commitment to delivering high-quality work.

• Provide constructive feedback to support team development and shared success.

Skills and Qualifications

• PhD in Biostatistics or related field with 5+ years of industry experience, or MS with 7+

years.

• Experience in oncology drug development preferred.

• Strong knowledge of FDA, EMA, and ICH guidelines, and a solid understanding of the end-to-

end drug development process.

• Expertise in statistical methods for clinical trials, up to date knowledge of statistical

applications and the ability to communicate complex concepts clearly to diverse audiences.

• Proficiency in SAS and R, and familiarity with CDISC SDTM and ADaM standards.

• Experience contributing to NDAs, MAAs, or other global regulatory submissions.

• Ability to collaborate effectively with CRO partners and manage outsourced statistical

activities.

• Strong interpersonal and communication skills, with the ability to build trust and guide

cross-functional decision-making.

• Demonstrated accountability, strong analytical thinking, and a data-driven approach to

problem-solving.

• Ability to work both independently and within a collaborative, matrixed team environment.

• Sense of urgency, initiative, and adaptability in a fast-moving, small-company setting.

• Excellent organizational, time management, and project leadership skills.

• High attention to detail and strong problem-solving capabilities.

• Willingness to learn, grow, and contribute to Company’s mission.

Working Behaviors (Core Expectations)

• Trust and Respect: Act with integrity, honesty, and openness to build strong, credible

relationships.

• Communication and Feedback: Share information clearly, listen actively, and engage in a

culture of constructive feedback.

• Accountability and Reliability: Take ownership for performance, be dependable, and support

others to achieve collective goals.

• Objectivity: Align on common objectives and use facts and data to reach fair, effective

decisions.

• Team Balance and Enablement: Contribute to balanced roles within the team, support

delegation, and help colleagues reach their full potential.