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Senior Statistical Programmer Analyst Jobs (NOW HIRING)

Collabera

Statistical Programmer/Analyst

Greenville, SC · On-site

Statistical Programmer/Analyst Location: Greenville, SC Duration: 12+ Months (could go beyond) Responsibilities: Interpret large amounts of data, analyze results using statistical methods, interpret ...

Syneoshealth

Sr Statistical Programmer (NA Only)

Sr Statistical Programmer (NA Only) Syneos Health is a leading fully-integrated life sciences ... Reviews project documentation such as Statistical Analysis Plan, mock shells, programming ...

Intego Group

NY · On-site

$90 - $120/hr

Senior/Principal Clinical Statistical Programmer USA Intego Clinical's office in Florida, USA, is ... Validate the work of other programmers/analysts. * Create/review programming plan, specifications ...

SystImmune, Inc.

$80 - $100/hr

The Statistical Programmer will support statistical programming activities for clinical trials ... Review study documents including statistical analysis plans (SAPs), CRFs, database specifications ...

New

BeiGene, Ltd.

$144 - $189/hr

General Description:**The (Senior) Principal Programmer works within BeOne's Statistical ... Analytical Thinking/Data Analysis* Financial Excellence* Communicates with ClaritySalary Range ...

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How much do senior statistical programmer analyst jobs pay per year?

As of Sep 6, 2026, the average yearly pay for senior statistical programmer analyst in the United States is $128,293.00, according to ZipRecruiter salary data. Most workers in this role earn between $107,000.00 and $148,000.00 per year, depending on experience, location, and employer.

What does a senior statistical programmer analyst do?

A Senior Statistical Programmer Analyst is responsible for designing, developing, and validating statistical programs that analyze clinical trial or research data. They work closely with biostatisticians and data managers to ensure data accuracy, integrity, and compliance with regulatory standards. Their work includes creating tables, listings, and figures (TLFs), developing analysis datasets, and automating data processes. Senior Statistical Programmer Analysts often mentor junior programmers and play a key role in quality control and project delivery within pharmaceutical, biotechnology, or clinical research organizations.

How does a senior statistical programmer analyst typically collaborate with cross-functional teams in clinical research projects?

As a Senior Statistical Programmer Analyst, you will regularly collaborate with biostatisticians, data managers, clinical research associates, and project managers. Your main responsibility is to translate statistical analysis plans into programming code (often using SAS or R), ensuring datasets and outputs meet regulatory standards. You’ll participate in team meetings to clarify study requirements, address data or programming issues, and ensure timelines are met. Strong communication and documentation skills are essential, as you often serve as a bridge between technical and non-technical team members.

What are the key skills and qualifications needed to thrive as a senior statistical programmer analyst, and why are they important?

To thrive as a Senior Statistical Programmer Analyst, you need advanced programming skills in SAS or R, a strong background in statistics, and a relevant degree such as in mathematics, statistics, or computer science. Experience with clinical trial data, CDISC standards (SDTM, ADaM), and regulatory submission processes, along with certifications like SAS Certified Professional, are highly valued. Exceptional problem-solving abilities, attention to detail, and effective communication enable you to manage complex datasets and collaborate with cross-functional teams. These combined skills ensure accurate data analysis, regulatory compliance, and successful delivery of biostatistical projects in the pharmaceutical or clinical research industry.
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Senior Statistical Programmer Analyst jobs near you
Infographic showing various Senior Statistical Programmer Analyst job openings in the United States as of August 2026, with employment types broken down into 89% Full Time, 6% Part Time, and 5% Contract. Highlights an 82% Physical, 7% Hybrid, and 11% Remote job distribution, with an average salary of $128,293 per year, or $61.7 per hour.

Senior SAS/Statistical Programmer

Wizsolution

Plainsboro, NJ • Remote

Full-time

Re-posted 27 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