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Associate Director Sas Statistical Programming information

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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

Burlington, MA • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

$200 - $250/hr

Other

Posted 10 days ago

Job description

Position Summary

MBX is seeking an Associate Director, Statistical Programming to lead and contribute to statistical programming and analysis of clinical trial data.

What You’ll Do
  • Oversee and execute statistical programming deliverables for planned analyses (study monitoring, data reviews, clinical study reports, data integrations, regulatory query responses) across compounds and studies.
  • Lead global submission activities as a programming functional/technical expert; ensure deliverables meet timelines, quality, and regulatory expectations (ICH/FDA/EMA).
  • Manage CROs/contractors to ensure compliant, high-quality deliverables within timeline and budget.
  • Develop and validate reproducible, well-documented statistical programs for integrated scientific reports, aligned to protocols and Statistical Analysis Plans (SAPs) and regulatory conventions.
  • Maintain and enhance the internal SAS macro library and database.
  • Provide input to SAPs, publications, scientific presentations, regulatory submissions, and promotional materials.
  • Review CRFs/CRF annotations, SAPs, TLF shells and outputs, and dataset specifications (SDTM/ADaM).
  • Lead statistical programming within study teams; communicate statistical/programming issues to development teams.
  • Contribute to programming standards, macros, SOPs, and process improvements.
  • Other responsibilities as assigned.
What You Bring
  • 8+ years statistical programming experience in biotech/pharma (preferred: endocrine/metabolic disorders).
  • Advanced degree (PhD/MS/etc.) preferred.
  • Proficient in SAS (Base SAS, SAS/Stat, SAS/Graph, macros, ODS) and solid understanding of database systems.
  • R and Python experience preferred.
  • CDISC experience (SDTM, ADaM, define.xml) and eCTD/eSub submissions.
  • Ability to lead programming and oversee CRO deliverables.
  • Strong analytical, organizational, communication skills; manage multiple priorities.
Travel & In Office Presence
  • Periodic travel and hybrid work schedule based on business needs/office practices.
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