Experienced I Statistical Programmer

Johnson & Johnson · Bangalore, India +2 more

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Role summary

Johnson & Johnson seeks an experienced statistical programmer to support clinical trial data analysis and reporting activities. The role involves designing and developing programs for low-to-medium complexity trials, ensuring CDISC compliance, and collaborating with cross-functional teams in India locations.

Where this listing comes from

This listing was compiled by RoleLantern from the employer's publicly available posting on Workday, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-06 (originally posted 2026-10-05). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.

What they're looking for

Bachelor's degree in computer science, data science, mathematics, public health, or related scientific field
2+ years programming experience in pharmaceutical, biotech, or CRO industry
Proficiency in R language and safety programming
Knowledge of SAS, Python, or similar languages for data manipulation and statistical analysis
Basic understanding of regulatory guidelines (ICH-GCP) and clinical R&D concepts
Strong written and verbal communication skills
Experience working in team environments

What you'll be doing

Design and develop programs supporting clinical research analysis and reporting activities
Lead or complete programming activities for trials of low to medium complexity with quality and timeliness
Verify programming and reporting outputs; review project requirements and documentation
Create and verify CDISC-compliant data packages and submission materials for regulatory review
Collaborate with team members and cross-functional partners including statistics, clinical, and regulatory groups

Privacy & handoff

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Date posted1 day ago

Last source checkToday

Salary listedNeeds clarity

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