Statistical Programmer

Johnson & Johnson

. Complete and may lead programming trial activities of low to medium complexity and/or criticality, with high quality and timeliness of deliverables .

Posted 10/4/2026full-timeBangalore • IndiaJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in programming for clinical research analysis and reporting, with proficiency in SAS, R, and Python. Maintains compliance with regulatory guidelines and contributes to process improvement within a collaborative team environment.

Highest-signal resume keywords

SAS ProgrammingR Language ProficiencyPython ProgrammingClinical Research KnowledgeRegulatory Guidelines Compliance

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

ProgrammingData ManipulationStatistical AnalysisVerification of Programming ActivitiesCDISC Compliance

Soft Skills

Excellent Communication SkillsTeam Collaboration

Industry Keywords

Pharmaceutical IndustryCROBiotechICH-GCPClinical R&D

Tech Stack

Tools & technologies

Python

About the role

Key responsibilities & impact

Complete and may lead programming trial activities of low to medium complexity and/or criticality, with high quality and timeliness of deliverables
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, use the latest standards, and deploy current 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 business/operational processes
Report to a people manager within the Delivery Unit and remain accountable to Portfolio and Study Leads
Collaborate with internal functional contacts, 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)
Approx. 2+ years of relevant programming experience, preferably in Pharmaceutical, CRO or Biotech industry or related field or industry
Basic knowledge of regulatory guidelines (e.g. ICH-GCP) and relevant clinical R&D concepts
Experience working in a team environment preferred
Excellent written and verbal communications skills
Knowledge of data structures and relevant programming languages for data manipulation/statistical analysis and reporting, including SAS, R, Python, etc.
Basic knowledge of processes, methods, and concepts relevant to programming
R language and safety experience
SAS knowledge preferred for Clinical Programming role

Benefits

Comp & perks

Inclusive work environment
Respect for diversity and dignity of employees
Employee merit recognition