Statistical Programmer

Everest Clinical Research

. Develop and review SDTM and ADaM dataset specifications, annotated CRFs, define.xml, reviewer’s guides, and related documents .

Posted 10/6/2026full-timeBridgewater • New Jersey • United StatesJuniorMid-Level💰 $80,000 - $116,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in statistical programming for clinical trials, including proficiency in SAS, R, and SQL, while ensuring compliance with CDISC standards and regulatory requirements. Capable of developing and validating datasets, generating statistical reports, and maintaining data integrity throughout the clinical research process.

Highest-signal resume keywords

SAS ProgrammingStatistical Programming SupportCDISC Conformance ChecksClinical Trial Statistical ProgrammingData Integrity Checks

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

SASRSQLExcelStatistical Output ReportsSDTM DatasetsADaM DatasetsData ListingsSummary TablesGraphs

Tools & Technologies

Statistical Analysis SoftwareDatabase Management

Industry Keywords

Clinical TrialsPharmaceutical ResearchRegulatory ComplianceData ManagementAudit Readiness

Tech Stack

Tools & technologies

SQL

About the role

Key responsibilities & impact

Develop and review SDTM and ADaM dataset specifications, annotated CRFs, define.xml, reviewer’s guides, and related documents
Program and validate SDTM and ADaM datasets
Perform CDISC conformance checks and address findings
Develop SAS programs for statistical output reports based on SAP and TLG mock-up shells
Provide statistical programming support for Clinical Study Reports, integrated safety and efficacy analyses, regulatory safety reports, ad-hoc requests, and exploratory data analyses
Develop and maintain SAS programs for database integrity checks and ongoing data cleaning
Work with Data Managers to address data issues and queries
Reconcile CRF and non-CRF data and perform non-CRF data integrity checks
Generate data listings, summary tables, graphs, and Patient Profiles
Document data and programming information according to SOPs and Working Instructions
Achieve audit readiness for internal and external quality and compliance audits
Meet Everest and Sponsor-specific statistical programming KPIs
Develop expertise in other programming and system administration areas when required

Requirements

What you’ll need

Master’s or higher in statistics, biostatistics, or a related quantitative field
At least two years of experience in clinical trial statistical programming
Working knowledge of SAS, R, SQL, and Excel
Must pass a SAS-based assessment test
Must work remotely from a home-based office anywhere in the USA or work onsite in Bridgewater, New Jersey
Comply with Everest company-specific and clinical trial Sponsor-specific training requirements
Maintain current knowledge of pharmaceutical clinical research industry standards, conventions, and regulatory requirements
Knowledge of clinical trial Sponsor-specific requirements when applicable

Benefits

Comp & perks

Medical, dental, and vision coverage
Life and AD&D insurance
Short- and long-term disability
Tuition reimbursement
Fitness reimbursement
Employee assistance program (EAP)
401(k) retirement plan
Generous paid time off and sick leave
Opportunity to earn a performance-based bonus
Remote work from a home-based office in the USA in accordance with the Work from Home policy