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Statistical Programmer Jobs in Jacksonville, FL (NOW HIRING)

Adhere to NCAA, conference, and institutional statistical guidelines. * Maintain focus and composure in high-pressure, live-event settings. * Assist with post-game stat corrections or uploads as ...

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

Proficiency in statistical programming languages such as R, Python, SAS, or similar, alongside general programming and SQL knowledge. * Demonstrated experience building and deploying statistical and ...

Quality Engineer

Jacksonville, FL · On-site

$66K - $86K/yr

Kavaliro is seeking a detail-oriented Quality Engineer to support the development, implementation ... Product Quality & Statistical Analysis * Evaluate product quality through statistical analysis ...

Quality Engineer

Jacksonville, FL · On-site

$40 - $44.22/hr

Quality Engineer Full-time Jacksonville, FL, US Exclusive confidential search -- details shared ... Design and apply statistical methods, sampling plans, and control charts to assess and improve ...

Quality Engineer

Orange Park, FL

$59K - $76K/yr

Job Summary The Quality Engineer is responsible for ensuring aerospace hose products meet all ... Statistical Process Control (SPC) and data analysis * Risk assessment and quality planning

Quality Engineer

Orange Park, FL · On-site

$59K - $76K/yr

Job Summary The Quality Engineer is responsible for ensuring aerospace hose products meet all ... Statistical Process Control (SPC) and data analysis * Risk assessment and quality planning

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Statistical Programmer information

See Jacksonville, FL salary details

$78.3K

$136.5K

$230.7K

How much do statistical programmer jobs pay per year?

As of Aug 22, 2026, the average yearly pay for statistical programmer in Jacksonville, FL is $136,475.00, according to ZipRecruiter salary data. Most workers in this role earn between $115,800.00 and $148,200.00 per year, depending on experience, location, and employer.

What is a statistical programmer?

Statistical programmers are professionals who use statistical software and programming languages, such as SAS, R, or Python, to manage, analyze, and report data, often in clinical trials, public health, or research settings. They play a crucial role in transforming raw data into meaningful results by writing code for data cleaning, data manipulation, statistical analysis, and generating reports. Statistical programmers often work closely with statisticians, data managers, and researchers to ensure the accuracy and integrity of data analyses. Their work is essential in industries like pharmaceuticals, healthcare, and academia.

What does a statistical programmer do?

A statistical programmer creates statistical programming deliverables. You ensure excellent programming of analysis-ready data, tables, and figures. You may use Stata for general purpose statistical analysis or SPSS for interactive or batched statistical analysis. Your responsibilities include developing standard operating procedures and complying with guidelines. Other duties include remaining informed on developments in programming standards and meeting all regulatory requirements. You also create PROC statements that call upon named procedures for analysis. You develop programs for dataset integration, prepare resource plans, and assist with quality control of datasets.

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

To thrive as a Statistical Programmer, you need a strong background in statistics, data analysis, and programming—typically with a degree in statistics, mathematics, computer science, or a related field. Expertise in statistical software such as SAS, R, or Python and familiarity with data management systems like CDISC or SQL are often required, along with relevant certifications. Strong problem-solving abilities, attention to detail, and clear communication skills help you interpret data accurately and collaborate effectively with cross-functional teams. These skills ensure the delivery of high-quality, reproducible statistical analyses crucial for informed decision-making in research and industry settings.

What are some common challenges faced by statistical programmers when working on clinical trial data?

Statistical Programmers often encounter challenges such as managing large, complex datasets, ensuring data integrity, and adhering strictly to regulatory standards (like CDISC SDTM and ADaM). They must also collaborate closely with biostatisticians and data managers to accurately translate statistical analysis plans into code. Tight project timelines and shifting priorities can require strong organizational skills and adaptability. Effective communication and attention to detail are essential for navigating these challenges and delivering reliable results.

What is the difference between Statistical Programmer vs Data Analyst?

AspectStatistical ProgrammerData Analyst
Required CredentialsBachelor's in Statistics, Biostatistics, or related field; experience with SAS, R, or PythonBachelor's in Statistics, Data Science, or related field; proficiency in Excel, SQL, and visualization tools
Work EnvironmentPharmaceutical, clinical research, or healthcare industries; focus on programming and data managementVarious industries including finance, marketing, healthcare; focus on data interpretation and reporting
Employer & Industry UsageCommon in clinical trials, biotech, pharma companiesUsed across multiple sectors like finance, retail, and healthcare

While both roles handle data, Statistical Programmers primarily focus on programming and managing clinical or research data, whereas Data Analysts interpret data to generate insights across various industries. The roles often overlap in skills like statistical software proficiency but differ in their core responsibilities and industry focus.

What are the most commonly searched types of Statistical Programmer jobs in Jacksonville, FL?

The most popular types of Statistical Programmer jobs in Jacksonville, FL are:

What are popular job titles related to Statistical Programmer jobs in Jacksonville, FL?

For Statistical Programmer jobs in Jacksonville, FL, the most frequently searched job titles are:

What job categories do people searching Statistical Programmer jobs in Jacksonville, FL look for?

The top searched job categories for Statistical Programmer jobs in Jacksonville, FL are:

What cities near Jacksonville, FL are hiring for Statistical Programmer jobs?

Cities near Jacksonville, FL with the most Statistical Programmer job openings:

Infographic showing various Statistical Programmer job openings in Jacksonville, FL as of August 2026, with employment types broken down into 1% Internship, 82% Full Time, 14% Part Time, and 3% Contract. Highlights an 83% Physical, 3% Hybrid, and 14% Remote job distribution, with an average salary of $136,475 per year, or $65.6 per hour.

Information Technology_USA - USA_Data Scientist

Real Soft, Inc.

Jacksonville, FL • On-site

Contractor

Re-posted 11 days ago


Job description

Local to Raleigh, NC Only!
Role Overview
We are seeking a highly experienced Senior Statistical Programmer / Clinical Data Architect with 15+ years of expertise in clinical data programming, CDISC standards, and cloud-based analytics platforms. The ideal candidate will lead end-to-end clinical data workflows, regulatory submissions, and modern data platform transformations in GxP-regulated environments.
This role requires strong domain expertise in SDTM, ADaM, regulatory submissions, and SAS/Python/R programming, combined with experience in cloud platforms (AWS/Azure) and clinical data modernization initiatives.
Key Responsibilities
Clinical Data Programming & Regulatory Submissions
• Design, develop, and validate SDTM and ADaM datasets in compliance with CDISC standards
• Lead generation of define.xml, aCRF/eCRF annotations, and submission-ready deliverables
• Develop and optimize automated submission pipelines for FDA and global regulatory authorities
• Ensure compliance with GxP, 21 CFR Part 11, HIPAA, and ICH E6 guidelines
Data Engineering & Automation
• Architect and implement end-to-end clinical data pipelines using SAS, Python, and R
• Develop reusable SAS macro libraries and automation frameworks
• Build scalable data pipelines including modern formats (JSON/XPT alternatives)
• Drive migration from legacy systems to modern data architectures
Cloud & Platform Engineering
• Lead implementation and optimization of SAS Viya platforms on AWS/Azure
• Manage cloud infrastructure components (EKS, EC2, EFS, FSx, Databricks, etc.)
• Implement FinOps practices for cost governance and optimization
• Evaluate and onboard next-gen analytics platforms (e.g., Databricks)
Leadership & Stakeholder Management
• Lead cross-functional teams across US, UK, and offshore locations
• Collaborate with clinical, statistical, regulatory, and IT stakeholders
• Drive Agile delivery and sprint planning for data and platform initiatives
• Manage vendor relationships, tool selection, and licensing strategies
Compliance & Governance
• Ensure adherence to regulatory and audit requirements (FDA, OCC, SOX, Basel III as applicable)
• Maintain audit-ready documentation and validation processes
• Implement data governance, traceability, and reproducibility standards
Required Qualifications
• Bachelor's or Master's degree in Computer Science, Statistics, Life Sciences, or related field
• 15+ years of experience in statistical programming and clinical data management
• Strong expertise in:
o SAS (Base, Macro, SQL, ODS, STAT, Graph)
o CDISC standards (SDTM, ADaM, define.xml)
o Regulatory submissions (FDA, global agencies)
• Hands-on experience with:
o Python (Pandas) and/or R (admiral, Shiny)
o Cloud platforms (AWS/Azure)
• Strong understanding of GxP and clinical compliance frameworks
Preferred Qualifications
• Experience with SAS Viya architecture and administration
• Familiarity with Databricks, DBT, or modern data engineering tools
• Knowledge of CI/CD tools (Jenkins, Git)
• Experience in financial/regulatory environments (Basel III, CCAR, OCC) is a plus
• AWS or cloud certifications
Key Skills
• Clinical Data Standards: SDTM, ADaM, CDISC
• Programming: SAS, Python, R, SQL
• Cloud: AWS, Azure
• Tools: Pinnacle 21, Git, Jenkins, Power BI, Grafana
• Methodologies: Agile, DevOps, Data Governance
Role Descriptions: Key ResponsibilitiesClinical Data Programming & Regulatory SubmissionsDesign| develop| and validate SDTM and ADaM datasets in compliance with CDISC standardsLead generation of define.xml| aCRF/eCRF annotations| and submission-ready deliverablesDevelop and optimize automated submission pipelines for FDA and global regulatory authoritiesEnsure compliance with GxP| 21 CFR Part 11| HIPAA| and ICH E6 guidelinesData Engineering & AutomationArchitect and implement end-to-end clinical data pipelines using SAS| Python| and RDevelop reusable SAS macro libraries and automation frameworksBuild scalable data pipelines including modern formats (JSON/XPT alternatives)Drive migration from legacy systems to modern data architecturesCloud & Platform EngineeringLead implementation and optimization of SAS Viya platforms on AWS/AzureManage cloud infrastructure components (EKS| EC2| EFS| FSx| Databricks| etc.)Implement FinOps practices for cost governance and optimizationEvaluate and onboard next-gen analytics platforms (e.g.| Databricks)Leadership & Stakeholder ManagementLead cross-functional teams across US| UK| and offshore locationsCollaborate with clinical| statistical| regulatory| and IT stakeholdersDrive Agile delivery and sprint planning for data and platform initiativesManage vendor relationships| tool selection| and licensing strategiesCompliance & GovernanceEnsure adherence to regulatory and audit requirements (FDA| OCC| SOX| Basel III as applicable)Maintain audit-ready documentation and validation processesImplement data governance| traceability| and reproducibility standardsRequired QualificationsBachelors or Masters degree in Computer Science| Statistics| Life Sciences| or related field15+ years of experience in statistical programming and clinical data managementStrong expertise in: oSAS (Base| Macro| SQL| ODS| STAT| Graph)oCDISC standards (SDTM| ADaM| define.xml)oRegulatory submissions (FDA| global agencies)Hands-on experience with: oPython (Pandas) and/or R (admiral| Shiny)oCloud platforms (AWS/Azure)Strong understanding of GxP and clinical compliance frameworksPreferred QualificationsExperience with SAS Viya architecture and administrationFamiliarity with Databricks| DBT| or modern data engineering toolsKnowledge of CI/CD tools (Jenkins| Git)Experience in financial/regulatory environments (Basel III| CCAR| OCC) is a plusAWS or cloud certificationsKey SkillsClinical Data Standards: SDTM| ADaM| CDISCProgramming: SAS| Python| R| SQLCloud: AWS| AzureTools: Pinnacle 21| Git| Jenkins| Power BI| GrafanaMethodologies: Agile| DevOps| Data Governance
Essential Skills: Key ResponsibilitiesClinical Data Programming & Regulatory SubmissionsDesign| develop| and validate SDTM and ADaM datasets in compliance with CDISC standardsLead generation of define.xml| aCRF/eCRF annotations| and submission-ready deliverablesDevelop and optimize automated submission pipelines for FDA and global regulatory authoritiesEnsure compliance with GxP| 21 CFR Part 11| HIPAA| and ICH E6 guidelinesData Engineering & AutomationArchitect and implement end-to-end clinical data pipelines using SAS| Python| and RDevelop reusable SAS macro libraries and automation frameworksBuild scalable data pipelines including modern formats (JSON/XPT alternatives)Drive migration from legacy systems to modern data architecturesCloud & Platform EngineeringLead implementation and optimization of SAS Viya platforms on AWS/AzureManage cloud infrastructure components (EKS| EC2| EFS| FSx| Databricks| etc.)Implement FinOps practices for cost governance and optimizationEvaluate and onboard next-gen analytics platforms (e.g.| Databricks)Leadership & Stakeholder ManagementLead cross-functional teams across US| UK| and offshore locationsCollaborate with clinical| statistical| regulatory| and IT stakeholdersDrive Agile delivery and sprint planning for data and pla, Project Code :