Johnson & Johnson (J&J) has announced an opportunity for an Experienced I Statistical Programmer under its Data Analytics & Computational Sciences function in India. The position is available across Bangalore, Mumbai and Penjerla, Telangana, with a hybrid work arrangement.

This Johnson & Johnson Statistical Programmer job is suitable for candidates with a Bachelor’s degree or higher in Computer Science, Data Science, Data Engineering, Mathematics, Public Health or another relevant scientific discipline. Candidates should have approximately 2+ years of relevant programming experience, preferably within the pharmaceutical, CRO, biotech or related industry.

Professionals with knowledge of SAS, R, Python, clinical trials, CDISC, statistical programming and clinical data reporting should consider this opportunity.

Johnson & Johnson Statistical Programmer Job Overview

About the Experienced Statistical Programmer Role

The Experienced I Statistical Programmer works within Johnson & Johnson’s Integrated Data Analytics and Reporting (IDAR) organization.

The position supports programming, data analysis and reporting activities associated with clinical trials. The selected candidate will use knowledge of data structures, programming languages, industry standards and statistical programming methods to support clinical research.

The programmer may work on one or more clinical trials of low to medium complexity or criticality while contributing to data analysis, regulatory submission deliverables and process-improvement initiatives.

Key Responsibilities

As an Experienced Statistical Programmer at Johnson & Johnson, responsibilities may include:

• Completing and potentially leading programming activities for clinical trials of low to medium complexity or criticality.
• Designing and developing programs supporting clinical research analysis and reporting.
• Performing verification of programming and reporting activities.
• Reviewing project requirements, specifications and relevant documentation.
• Supporting regulatory submission activities.
• Creating, verifying and delivering CDISC-compliant data packages and other required data deliverables.
• Supporting preparation of reviewer guides.
• Following departmental programming processes, procedures and current standards.
• Applying appropriate technologies and programming standards to assigned clinical trial activities.
• Collaborating with programming and cross-functional clinical research teams.
• Contributing to departmental innovation and process improvement projects.
• Maintaining compliance with required company training and operational processes.

Clinical Programmer Responsibilities

For candidates working within the Clinical Programmer function, responsibilities can additionally include reviewing specifications for mapping Johnson & Johnson’s internal Data Review Model (DRM) and ensuring appropriate verification.

The Statistical Programmer may also:

• Program edit checks to support clinical data cleaning.
• Develop data review listings.
• Create clinical data visualizations.
• Generate listings for Data Management.
• Support Medical Monitoring reporting requirements.
• Support Central Monitoring activities.
• Review data structures for fit-for-purpose reporting.

These responsibilities make the position particularly relevant for professionals interested in SAS clinical programming, clinical data analysis, CDISC and pharmaceutical statistical programming.

Educational Qualification

Johnson & Johnson requires a Bachelor’s degree or higher and/or equivalent in one of the following areas:

• Computer Science
• Data Science / Data Engineering
• Mathematics
• Public Health
• Another relevant scientific field
• Equivalent theoretical or technical discipline

Candidates with higher qualifications in relevant disciplines can also apply if they meet the required technical and professional criteria.

Because the employer uses the broader wording “another relevant scientific field,” applicants from other scientific or life-science backgrounds should assess whether their academic training and programming experience provide the required theoretical and technical depth.

Experience Required

Candidates should have approximately 2+ years of relevant programming experience.

Experience in the following industries is preferred:

Pharmaceutical | CRO | Biotechnology | Clinical Research | Related industries

This is therefore an experienced-level opportunity rather than a fresher statistical programming vacancy.

Programming Skills Required

Candidates should understand data structures and programming languages used for data manipulation, statistical analysis and reporting.

Relevant programming technologies include:

• SAS
• R
• Python

The job description specifically states that SAS knowledge is preferred for the Clinical Programming role.

Applicants targeting clinical SAS programming careers should therefore prominently highlight SAS programming, clinical trial datasets, statistical analysis and relevant reporting experience on their CV.

Other Skills & Knowledge

Candidates should preferably demonstrate knowledge or experience in:

• Statistical Programming
• Clinical Trials
• Biostatistics
• CDISC
• Clinical Data Reporting
• Data Modeling
• Data Quality
• Statistical Analysis
• ICH-GCP
• Clinical R&D concepts
• Advanced Analytics
• Data Privacy Standards
• Analytical Reasoning
• Report Writing
• Research Ethics

Excellent written and verbal communication skills and the ability to collaborate effectively in a team environment are also important.

Who Can Apply?

This Johnson & Johnson Experienced Statistical Programmer job could be particularly relevant for professionals working as:

• Statistical Programmer
• Clinical SAS Programmer
• Clinical Programmer
• SAS Programmer
• Statistical Programming Analyst
• Clinical Data Programmer
• Biostatistical Programmer
• Clinical Data Analyst

Candidates should have relevant programming expertise and approximately two or more years of applicable professional experience.

Why Consider This Johnson & Johnson Opportunity?

The position provides exposure to programming activities supporting clinical research and pharmaceutical development within a major global healthcare organization.

The role offers opportunities to work across clinical trial programming, statistical analysis, CDISC data packages, regulatory submissions, clinical data cleaning and reporting.

The programmer also collaborates with functions such as Data Management, Central Monitoring, Statistics, Clinical, Global Medical Safety, Regulatory, Regulatory Medical Writing and Project Management.

The employer describes its workplace as inclusive and focused on healthcare innovation and professional collaboration.

Job Locations and Work Model

The Experienced I Statistical Programmer position is listed for:

Bangalore, Karnataka
Mumbai, Maharashtra
Penjerla, Telangana

The employer identifies the working arrangement as Hybrid Work.

Candidates should check the official posting for current workplace attendance requirements before applying.

How to Apply

Application Link