Experienced Statistical Programmer

Johnson & Johnson

. Complete and potentially lead programming trial activities of low to medium complexity and/or criticality .

Posted 10/15/2026full-timePENJERLA • IndiaJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in programming for clinical research, with a strong focus on SAS, R, or Python for data manipulation and statistical analysis. Capable of ensuring compliance with CDISC standards and regulatory guidelines while contributing to process improvements and team collaboration.

Highest-signal resume keywords

SAS ProgrammingClinical Trial ProgrammingCDISC ComplianceStatistical AnalysisRegulatory Guidelines Knowledge

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Programming LanguagesData ManipulationStatistical AnalysisClinical Research AnalysisVerification of Programming ActivitiesDocumentation ReviewProcess ImprovementData StructuresProgramming MethodsClinical R&D Concepts

Soft Skills

Excellent Communication SkillsTeam Collaboration

Industry Keywords

PharmaceuticalCROBiotechICH-GCPClinical TrialsData PackagesReviewer's Guides

Tech Stack

Tools & technologies

Python

About the role

Key responsibilities & impact

Complete and potentially lead programming trial activities of low to medium complexity and/or criticality
Design and develop programs supporting clinical research analysis and reporting
Perform appropriate verification of programming and reporting activities
Review and provide input for project requirements and documentation
Support submission activities, including creation, verification, and delivery of CDISC-compliant and/or non-standard data packages and reviewer’s guides
Follow departmental processes and procedures, current standards, and deployed technologies
Contribute to departmental innovation and process improvement projects
Collaborate with team and cross-functional members
Maintain compliance with company and departmental training, time reporting, and other operational processes
Report to a people manager within the Delivery Unit and remain accountable to Portfolio and Study Leads

Requirements

What you’ll need

Bachelor’s degree or higher and/or equivalent in computer science, data science/data engineering, mathematics, public health, or another relevant scientific field (or equivalent theoretical/technical depth)
Approximately 2+ years of relevant programming experience, preferably in Pharmaceutical, CRO, Biotech, or related industry
Basic knowledge of regulatory guidelines, such as ICH-GCP, and relevant clinical R&D concepts
Experience working in a team environment preferred
Excellent written and verbal communication skills
Knowledge of data structures and relevant programming languages for data manipulation, statistical analysis, and reporting, including SAS, R, or Python
SAS knowledge preferred for Clinical Programming role
Basic knowledge of processes, methods, and concepts relevant to programming
Ability to support programming activities for clinical trials of low to medium complexity/criticality
Knowledge of CDISC-compliant data packages and reviewer’s guides

Benefits

Comp & perks

Inclusive work environment
Employee respect, diversity, dignity, and merit recognition