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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 Jun 5, 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 are the key skills and qualifications needed to thrive as an Associate Director SAS Statistical Programming, and why are they important?

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 of 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 does an Associate Director of 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 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.

Infographic showing various Associate Director Sas Statistical Programming job openings in the United States as of May 2026, with employment types broken down into 89% Full Time, 4% Part Time, and 7% Contract. Highlights an 85% In-person, and 15% Remote job distribution, with an average salary of $119,333 per year, or $57.4 per hour.
Senior SAS/Statistical Programmer

Senior SAS/Statistical Programmer

Wizsolution

Plainsboro, NJ • Remote

Full-time

Posted 23 days ago

Job description

Job Description

Company Descriptions:

Wizsolution is located in Princeton NJ, which is a leader in pharmaceutical recruitment and staffing. Our goal is to provide effective solutions for fulfilling your career potential. The mission of our company is to connect high talent and motivated candidates to technical positions from our partner companies.

Job descriptions:

Senior SAS Programmer
Senior Statistical Programmer

*

-Perform SAS data manipulation and analysis programming
-May work with medical writing, clinical operations, and other clinical staff to support deliverables.
-Must work well both independently and with team members.
-Needs to be able to be on-time with deliverables, and for those deliverables to be of quality.
-Works with Statistician and Statistical programmer to assure results are consistent with expectations, and Quality control procedures are followed.
-Plans and carefully documents differences between programming results between program developer and Statistical QC programmer.
-Confirms that tracking sheets are current for projects, and may also confirm that results are consistent with earlier generated results.

·             MS with 3-5 +years of pharmaceutical industry experience.

·             Strong collaboration abilities and ability to work as part of a highly skilled team.

·             Experience in CDISC (SDTM, ADaM data sets)

·             Skilled in analysis of safety, efficacy & biomarker data, with an understanding of multiplicity issues; immunology/CV background a plus.

·             Experienced with standard and advanced statistical methods.

·             Expertise in SAS required, S-Plus or R preferred, including advanced statistical analysis, data integration, graphing & simulation.

·             Strong programming skills.

·             Good understanding of regulatory requirements & clinical trial design.

·             Knowledge of and ability to learn relevant clinical background and biomarker biology and incorporate these into statistical design, analysis & interpretation.

Preferred Qualifications:

Must have 3-5+ years SAS Programmer experience
SAS systems experience may include Base SAS, SAS/FSP,SAS SCL, Macro Facility, SAS/Graph, SAS / ODS, and SAS / Stat within a Windows operating system.

Job Type: Full-time