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Sas Programming Manager Jobs in Massachusetts (NOW HIRING)

LivaNova

Statistical Programmer II

Boston, MA · On-site

$90K - $100K/yr

Collaborate with Statistics, Data Management, Clinical, and vendor teams to clarify requirements and resolve data or programming issues. * Develop, validate, and maintain SAS programs in accordance ...

MMS

Senior Biostatistician - Remote (US)

Boston, MA · On-site

... supply management teams. * Develop phase 1-4 SAPs and make significant contributions to iSAPs ... Strong programming and logic skills (working knowledge of SAS) * Ability to apply drug development ...

Vrtx

Analytics CoE Senior Manager

Boston, MA

$144K - $216K/yr

The Senior Manager Director role is within HEOR's Analytics Center of Excellence (CoE), a ... Advanced proficiency in SAS programming and Excel required * Excellent written and oral ...

PhaseV

Biostatistics Researcher

Cambridge, MA · On-site

... proficiency in SAS programming is a plus * Experience in shell scripting, high performance ... Experience with leading and managing projects is preferred * Qualified candidates must be legally ...

PhaseV

Biostatistics Researcher

Cambridge, MA · On-site

... proficiency in SAS programming is a plus * Experience in shell scripting, high performance ... Experience with leading and managing projects is preferred * Qualified candidates must be legally ...

Zenas BioPharma

Senior Director, Biostatistics

Waltham, MA · Hybrid

$227K - $284K/yr

Proficiency in SAS programming and other statistical software tools. * Ability to manage people and projects * Comfortable working in a demanding, fast-paced, start-up culture with evolving processes.

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Sas Programming Manager information

What is a SAS programming manager?

SAS Programming Managers are professionals who oversee teams of SAS programmers, typically within the pharmaceutical, clinical research, or data analytics industries. Their responsibilities include project management, team leadership, and ensuring quality standards for statistical programming deliverables. They coordinate with other departments, manage timelines, and ensure that all data analysis and reporting using the SAS software adhere to regulatory and organizational requirements.

What are the key skills and qualifications needed to thrive as a SAS programming manager, and why are they important?

To thrive as a SAS Programming Manager, you need advanced SAS programming expertise, a solid background in statistics or data analysis, and typically a degree in a quantitative field with relevant management experience. Familiarity with clinical data management systems, regulatory standards (such as CDISC), and tools like SAS Base, Macro, and SQL is essential. Strong leadership, project management, and communication skills help you effectively lead teams and collaborate across departments. These competencies ensure the delivery of high-quality data outputs, regulatory compliance, and the successful management of complex projects.

What is the difference between Sas Programming Manager vs Sas Developer?

AspectSas Programming ManagerSas Developer
CredentialsBachelor's or Master's in Computer Science, Statistics, or related field; SAS certifications often preferredBachelor's in similar fields; SAS certifications beneficial
Work EnvironmentLeads teams, manages projects, collaborates with stakeholdersDevelops SAS programs, analyzes data, implements solutions
Industry UsageUsed in healthcare, finance, pharma for project oversightUsed across industries for data analysis and reporting
Search & ComparisonOften compared for leadership roles in SAS programmingFocuses on coding and data analysis tasks

The Sas Programming Manager oversees SAS projects and manages teams, while the Sas Developer primarily focuses on coding and data analysis. Both roles require SAS skills and certifications, but the manager role involves leadership and project management responsibilities, whereas the developer role emphasizes technical programming tasks.

What are some typical challenges faced by a SAS programming manager when leading a team of programmers in a clinical research setting?

A SAS Programming Manager in clinical research often encounters challenges such as balancing tight project timelines with data quality standards, coordinating cross-functional communication between statisticians, data managers, and regulatory teams, and ensuring team members stay updated on evolving industry regulations (like CDISC standards). Managing a diverse team with varying experience levels also requires strong mentorship and effective delegation to ensure consistent deliverables. Addressing these challenges proactively helps maintain project momentum and fosters professional growth within the team.

What are the most commonly searched types of Sas Programming jobs in Massachusetts?

The most popular types of Sas Programming jobs in Massachusetts are:

What are popular job titles related to Sas Programming Manager jobs in Massachusetts?

For Sas Programming Manager jobs in Massachusetts, the most frequently searched job titles are:

What job categories do people searching Sas Programming Manager jobs in Massachusetts look for?

The top searched job categories for Sas Programming Manager jobs in Massachusetts are:

Sas Programming Manager jobs near you
Infographic showing various Sas Programming Manager job openings in Massachusetts as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Associate Director, Statistical Programming

Zenas BioPharma

Waltham, MA • On-site

Full-time

Posted 18 days ago

Job description

Zenas is a clinical-stage global biopharmaceutical company committed to becoming a leader in the development and commercialization of transformative therapies for patients with autoimmune diseases. Our core business strategy combines our experienced leadership team with a disciplined product candidate acquisition approach to identify, acquire and develop product candidates globally that we believe can provide superior clinical benefits to patients living with autoimmune diseases. Zenas is advancing two late-stage, potential franchise molecules, obexelimab and orelabrutinib. Obexelimab, Zenas' lead product candidate, is a bifunctional monoclonal antibody designed to bind both CD19 and FcγRIIb, which are broadly present across B cell lineage, to inhibit the activity of cells that are implicated in many autoimmune diseases without depleting them. We believe that obexelimab's unique mechanism of action and self-administered, subcutaneous injection regimen may broadly and effectively address the pathogenic role of B cell lineage in chronic autoimmune disease. Orelabrutinib is a potentially best-in-class, highly selective CNS-penetrant, oral, small molecule Bruton's Tyrosine Kinase (BTK) inhibitor with the potential to address compartmentalized inflammation and disease progression in Multiple Sclerosis (MS). Zenas' earlier stage programs include ZB021, a clinical-stage, potentially best-in-class, oral, IL-17AA/AF inhibitor; ZB022, a preclinical, potentially best-in-class, oral, brain-penetrant, TYK2 inhibitor; and ZB014, a preclinical half-life extended anti-CD-19 and FcγRIIb monoclonal antibody.
We are seeking top talent who share our commitment to patients and have a track record of success in acquiring, developing and commercializing products across the globe. Our colleagues have an opportunity to engage in a fast-paced learning environment and experience individual and organizational success as we work towards becoming a global immunology and autoimmune disease leader, while living our values of Transparency, Relationships, Urgency, Excellence and Innovation - TRUE Innovation!
Position Summary:
The Associate Director, Statistical Programming will independently lead and execute programming activities aligned with project strategies to support clinical studies, study reports, and regulatory submissions. This role extends beyond study support to include strategic contributions to departmental infrastructure, such as process optimization and tool development. The position also involves direct management and oversight of internal, contract, and FSP programming resources.
Key Responsibilities:
  • Act as the primary statistical programming contact and knowledge expert for assigned protocols, studies, and integrated analyses.
  • Provide oversight of statistical programming activities, including those of internal staff, CROs, and FSP teams. Ensure deliverables meet quality standards, study timelines, and agreed scope.
  • Collaborate across functions (e.g., Biostatistics, Data Management, Clinical Operations) to provide expert programming support and strategic input.
  • Lead or contribute to departmental initiatives for process improvement, standardization, and the development or implementation of programming tools and macros to enhance efficiency and quality.
  • Review and provide expert input on SDTM and ADaM specifications, datasets, define.xml, reviewers guides, and validation reports.
  • Perform QC of SDTM datasets, ADaM datasets, and Tables, Figures, and Listings (TFLs).
  • Program TFLs for ad hoc analyses, posters, publications, and regulatory interactions.
  • Participate in the review of clinical study protocols, statistical analysis plans, and mock TFL shells.
  • Mentor, guide, and provide line management to junior programmers and assigned contract/FSP resources.
  • Manage relationships and performance with contract programming resources and Functional Service Providers (FSP).

Qualifications:
  • Master's degree in Biostatistics, Computer Science or related discipline, 7+ years' experience working across all phases of clinical trials in CRO/Biotech/ Pharmaceutical company; or Bachelor's degree with 9+ years of relevant experience.
  • Experience managing CROs and vendors.
  • NDA/BLA and other regulatory filing experience.
  • Experience with ISS/ISE.
  • Strong knowledge of CDISC standards for SDTM and ADaM.
  • Strong knowledge of ICH, FDA, EMA, and NMPA regulations and guidelines.
  • Exceptional interpersonal skills and problem-solving capabilities.
  • Excellent oral and written communication skills.
  • Experience working with cross-functional teams.
  • Excellent SAS programming skills.
  • Experience with other statistical software tools (e.g., R) preferred.
  • Comfortable working in a demanding, fast-paced, start-up culture with evolving processes. Flexible and able to adapt to new situations as the business demands.
  • Demonstrates flexibility to work non-traditional work hours when needed, given international operations across time zones.

#LI-Hybrid
The position is eligible for a competitive compensation and benefits package.
Zenas is committed to fair and equitable compensation practices. The base salary pay range for this role is $171,500 to $214,423. Actual compensation packages will depend on various factors, including, but not limited to depth of experience, education, skillset, overall performance and/or location.
Zenas believes in providing a competitive compensation and benefits package to all employees. Our base salary is just one component of Zenas' competitive total rewards strategy that also includes annual performance bonus, equity, full range of benefits and other incentive compensation plans.
Zenas BioPharma is proud to be an equal opportunity employer. We are committed to fostering an environment where diversity is valued. All qualified applicants will receive consideration for employment based on merit, qualifications and the needs of the business.

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