Experienced Statistical Programmer

Johnson & Johnson

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

Posted 9/29/2026full-timeMumbai • IndiaJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in programming for clinical research, including proficiency in SAS, R, or Python for data manipulation and statistical analysis. Strong understanding of regulatory guidelines and experience in data quality, reporting, and compliance within the pharmaceutical or biotech industries.

Highest-signal resume keywords

SAS ProgrammingStatistical AnalysisClinical TrialsData QualityGood Clinical Practice (GCP)

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

ProgrammingData ManipulationStatistical AnalysisData ModelingData VisualizationData CleaningAnalytical ReasoningAdvanced AnalyticsReport WritingBiostatistics

Soft Skills

Excellent Communication SkillsTeam Collaboration

Tools & Technologies

SASRPython

Industry Keywords

Clinical ResearchPharmaceuticalCROBiotechICH-GCPData Privacy StandardsResearch Ethics

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 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 operational processes
Review specifications for mapping the internal Data Review Model (DRM) for fit-for-purpose reporting consumption and ensure DRM verification
Support data cleaning through programmed edit checks and data review listings
Create data visualizations and listings for data management, medical monitoring, and central monitoring
Report to a people manager within the Delivery Unit and remain accountable to Portfolio and Study Leads
Collaborate with internal functional groups, Innovative Medicine peers, external partners, CRO management, vendor liaisons, industry peers, and working groups

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
Advanced Analytics
Analytical Reasoning
Biological Sciences
Biostatistics
Clinical Trials
Data Modeling
Data Privacy Standards
Data Quality
Data Savvy
Good Clinical Practice (GCP)
Report Writing
Research Ethics
Statistical Analysis Systems (SAS) Programming
Statistics
Technological proficiency

Benefits

Comp & perks

Inclusive work environment
Diversity and dignity of employees
Employee merit recognition