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Associate Director Sas Statistical Programming Jobs

OSI

$175K - $220K/yr

Associate Director, Statistical Programming The Associate Director, Statistical Programming will ... Expert‑level hands‑on experience with SAS programming in clinical trials; experience with R ...

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How much do associate director sas statistical programming jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for associate director sas statistical programming in the United States is $57.37, according to ZipRecruiter salary data. Most workers in this role earn between $21.15 and $85.34 per hour, depending on experience, location, and employer.

What does an associate director SAS statistical programming do?

An Associate Director of SAS Statistical Programming leads teams responsible for the design, development, and validation of statistical programming deliverables, primarily using SAS software, in clinical research or pharmaceutical settings. They oversee project timelines, ensure compliance with regulatory guidelines, and collaborate with biostatisticians, data managers, and other cross-functional teams. Additionally, they mentor programming staff, develop standard operating procedures, and contribute to process improvements to support successful submission of clinical study data.

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

To thrive as an Associate Director SAS Statistical Programming, you need advanced expertise in statistical programming, clinical data analysis, and a degree in statistics, mathematics, or a related field. Proficiency in SAS programming, CDISC standards (SDTM/ADaM), and experience with regulatory submission tools are typically required, along with relevant certifications. Strong leadership, project management, and communication skills set standout professionals apart in this role. These competencies ensure high-quality data deliverables, regulatory compliance, and effective team coordination in clinical research settings.

What are the typical challenges faced by an associate director SAS statistical programming when managing project timelines and deliverables?

An Associate Director of SAS Statistical Programming often manages multiple projects simultaneously, each with its own set of deadlines and requirements. One common challenge is balancing resource allocation while ensuring high-quality, compliant deliverables within tight timelines. Additionally, coordinating across cross-functional teams—such as biostatistics, data management, and clinical operations—requires strong communication and leadership skills. Staying updated on evolving regulatory standards and mentoring junior programmers are also key responsibilities that add to the complexity of the role.

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

AspectAssociate Director Sas Statistical ProgrammingSenior SAS Programmer
ResponsibilitiesOversees statistical programming teams, manages project timelines, and ensures regulatory complianceDevelops and validates SAS programs, supports statistical analyses, and maintains code quality
Required CredentialsBachelor's or Master’s in Biostatistics, Statistics, or related field; extensive SAS experience; leadership skillsBachelor's or Master’s in related field; strong SAS programming skills; relevant industry experience
Work EnvironmentLeadership role within clinical or pharmaceutical companies, often in cross-functional teamsHands-on programming within clinical research teams, often in CROs or pharma companies

The main difference is that the Associate Director Sas Statistical Programming holds a leadership position overseeing teams and projects, while the Senior SAS Programmer focuses on hands-on programming tasks. Both roles require strong SAS skills and industry experience, but the associate director role involves strategic oversight and team management.

Is SAS programming in demand?

SAS programming is in high demand in industries such as pharmaceuticals, healthcare, and finance, where it is used for data analysis and regulatory reporting. Skilled SAS programmers with knowledge of statistical methods and experience with tools like SAS Base and SAS Enterprise Guide are sought after, especially in roles involving clinical trials and data management.

What are popular job titles related to Associate Director Sas Statistical Programming jobs?

For Associate Director Sas Statistical Programming jobs, the most frequently searched job titles are:

Infographic showing various Associate Director Sas Statistical Programming job openings in the United States as of September 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $119,333 per year, or $57.4 per hour.

Associate Director, Statistical Programming

Waltham, MA

Kailera Therapeutics, Inc.
See more jobs at Kailera Therapeutics, Inc.external

Full-time

Re-posted 17 days ago

Job description

What You'll Do:

We are seeking an experienced programmer to join us as Associate Director, Statistical Programming. This is a critical role responsible for leading statistical programming activities on the assigned disease area(s). This role will support clinical trials, regulatory submissions, and other key initiatives.

Required location: Waltham, MA (hub-based, onsite 3-4 days per week)

Responsibilities:

  • Lead statistical programming efforts for clinical studies, including the development and review of programming specifications to ensure clarity, integrity, and compliance with internal and external standards
  • Lead the execution of ad-hoc and post-hoc analyses to support emerging clinical questions, publications, and internal decision-making
  • Oversee and coordinate activities with Contract Research Organizations (CROs), focusing on the implementation of CDISC standards, creation of SDTM, ADaM datasets, and TFLs, and ensuring high-quality deliverables
  • Conduct independent validation and quality checks of statistical programming deliverables from CROs
  • Collaborate closely with statisticians and cross-functional study teams to deliver results in a timely and accurate manner
  • Manage multiple projects simultaneously, ensuring tasks are prioritized effectively to meet deadlines

Required Qualifications:

  • Proven hands-on experience in programming for clinical development, preferably in a leadership role, with a strong preference for late-phase clinical trial support
  • Experience in regulatory submissions, including NDAs, BLAs, and other filings, with experience in ISS/ISE highly desirable
  • Expertise in SAS programming and comprehensive knowledge of CDISC standards
  • Familiarity with ICH/GCP guidelines and global regulatory submission requirements (e.g., FDA, EMA)
  • Extensive experience overseeing CROs, including independent validation of datasets and statistical deliverables

Preferred Qualifications:

  • Background in cardiometabolic diseases or related therapeutic areas is preferred

 

Education:

  • Advanced degree (MS/PhD) in Biostatistics, Statistics, or a related field
    • MS: Minimum of 8+ years of relevant experience
    • PhD: Minimum of 6+ years of relevant experience

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