Johnson & Johnson (J&J) is hiring for the position of Experienced I Statistical Programmer under its Data Analytics & Computational Sciences – Biostatistics function. The role is available in Bangalore, Mumbai, and Hyderabad and follows a hybrid work model.
This opportunity is intended for professionals with around 2+ years of relevant programming experience, preferably within the pharmaceutical, CRO, biotechnology, or related industries. The role supports clinical trial programming, data analysis, reporting, verification, and submission-related activities.
A key requirement mentioned in the vacancy is experience with the R programming language and safety-related work. Knowledge of SAS is preferred for Clinical Programming roles, while familiarity with other programming languages such as Python may also be relevant.
Johnson & Johnson Recruitment 2026 – Job Highlights
| Particulars | Details |
|---|---|
| Company | Johnson & Johnson |
| Job Title | Experienced I Statistical Programmer |
| Functional Area | Data Analytics & Computational Sciences |
| Sub Function | Biostatistics |
| Job Category | Scientific / Technology |
| Locations | Bangalore, Mumbai & Hyderabad |
| Work Model | Hybrid |
| Job Type | Full Time |
| Experience | Approx. 2+ years |
| Education | Bachelor’s degree or higher / equivalent |
| Key Requirement | R programming and safety experience |
| Preferred Programming | SAS, R, Python |
| Requisition ID | R-074782 |
| Application Deadline | October 14, 2026 |
| Salary / CTC | Not specified |
About Johnson & Johnson
Johnson & Johnson is a global healthcare company focused on healthcare innovation across areas including Innovative Medicine and MedTech.
The company works on healthcare solutions intended to address complex diseases and improve patient outcomes. The current opening is part of its Data Analytics & Computational Sciences organization and specifically supports biostatistics and clinical programming activities.
Job Description
The Experienced I Statistical Programmer is an individual contributor role within the programming team.
The position requires knowledge of data structures, programming methods, industry standards, and relevant programming languages. The selected candidate will support data analysis and reporting activities associated with clinical trials and may work on studies with low to medium levels of complexity or criticality.
The role also provides opportunities to contribute to process improvement and innovation initiatives within the programming organization.
Experienced I Statistical Programmer – Role Overview
The programmer will support clinical research activities through statistical programming, data analysis, reporting, quality verification, and submission-related programming deliverables.
The position may involve working independently on assigned activities while collaborating with programming, clinical, statistical, regulatory, data management, and other cross-functional teams.
Key Responsibilities
Clinical Trial Programming
The candidate will support programming activities for clinical trials, particularly studies with low to medium complexity or criticality.
Responsibilities include:
- Developing programs for clinical research analysis and reporting.
- Completing assigned programming deliverables within expected timelines.
- Supporting one or more clinical trials.
- Maintaining high-quality programming outputs.
- Following established programming processes and standards.
Program Development and Verification
The role includes designing and developing programs required for clinical research analyses.
The programmer will also:
- Perform appropriate verification of programming outputs.
- Support verification of reporting activities.
- Review project requirements.
- Provide input into relevant project documentation.
- Help maintain the quality and reliability of analytical deliverables.
Clinical Data and Submission Support
The position may contribute to regulatory submission activities, including:
- Creating CDISC-compliant data packages.
- Supporting non-standard data packages where required.
- Verifying submission-related programming outputs.
- Preparing or supporting reviewer’s guides.
- Following applicable data standards and submission requirements.
Standards and Process Compliance
The programmer will be expected to:
- Follow departmental processes and procedures.
- Use current programming and data standards.
- Apply available technologies appropriately.
- Complete required company and departmental training.
- Maintain accurate time reporting.
- Follow applicable business and operational procedures.
Innovation and Process Improvement
The role may also provide opportunities to contribute to:
- Departmental innovation projects.
- Programming process improvements.
- Technology or workflow enhancements.
- Initiatives designed to improve quality and efficiency.
Educational Qualification
Candidates should have a Bachelor’s degree or higher, or equivalent theoretical and technical knowledge, in a relevant field such as:
- Computer Science
- Data Science
- Data Engineering
- Mathematics
- Public Health
- Another relevant scientific discipline
Equivalent technical or theoretical depth may also be considered according to the job requirements.
Experience Requirements
The vacancy specifies approximately 2+ years of relevant programming experience.
Experience in one or more of the following environments is preferred:
- Pharmaceutical industry
- CRO
- Biotechnology
- Related healthcare or scientific field
Mandatory Experience Highlight
The supplied vacancy specifically states:
Experience with R language and safety is required.
Candidates should therefore have relevant exposure to R programming and safety-related activities before applying.
Required Technical Skills
Candidates should have knowledge of:
- R programming
- Statistical programming
- Data manipulation
- Data structures
- Clinical trial concepts
- Data analysis and reporting
- Programming verification
- Clinical research processes
- Regulatory requirements
- Good Clinical Practice
- Clinical data standards
Knowledge of SAS is preferred for Clinical Programming roles, while familiarity with programming languages such as Python may also be relevant.
Regulatory and Clinical Knowledge
The role requires basic understanding of regulatory and clinical research concepts, including:
- ICH-GCP
- Clinical Research & Development
- Clinical trials
- Data quality
- Research ethics
- Data privacy principles
- Clinical data standards
- Regulatory submission concepts
Preferred Skills
The vacancy lists several preferred skills, including:
- 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
- Research
- SAS Programming
- Statistics
- Technology proficiency
- Attention to detail
Communication and Collaboration Skills
The position involves working with multiple internal and external stakeholders. Candidates should therefore have:
- Strong written communication skills.
- Strong verbal communication skills.
- Ability to work effectively in a team.
- Cross-functional collaboration skills.
- Ability to communicate technical information clearly.
- Good organizational and documentation skills.
Work Location and Work Model
The position is available at the following locations:
- Bangalore, Karnataka
- Mumbai, Maharashtra
- Hyderabad, India
Work Model: Hybrid
The vacancy does not indicate that every candidate can select any location; candidates should confirm the applicable location during the application process.
Reporting and Collaboration
The role reports to a people manager within the Delivery Unit and works with Portfolio and Study Leads for assigned responsibilities.
The position may collaborate with teams and professionals across:
- Data Management
- Central Monitoring
- Programming
- Clinical Data Standards
- Regulatory Medical Writing
- Statistics
- Clinical teams
- Global Medical Safety
- Project Management
- Regulatory
- Strategic Partnerships
- Human Resources
External interaction may include CRO management, vendors, external partners, industry peers, and relevant working groups.
Salary / CTC
Johnson & Johnson has not specified the salary or CTC for this position in the supplied job posting.
Compensation details may depend on the candidate’s qualifications, experience, location, and applicable company policies.
Selection Process
The supplied vacancy does not provide a detailed step-by-step selection process.
Candidates should be prepared for potential screening, technical discussions, interviews, or other assessments based on the company’s recruitment process.
How to Apply for Johnson & Johnson Recruitment 2026
Interested and eligible candidates can apply online through the official Johnson & Johnson careers portal.
Job Requisition ID: R-074782
Application Deadline: October 14, 2026
Candidates should provide accurate information regarding their programming experience, particularly their R programming and safety-related experience.
Important Details Before Applying
- The position is for Experienced I Statistical Programmer.
- The role belongs to Data Analytics & Computational Sciences – Biostatistics.
- Work locations include Bangalore, Mumbai, and Hyderabad.
- The position follows a hybrid work model.
- Approximately 2+ years of relevant programming experience is mentioned.
- Pharmaceutical, CRO, biotechnology, or related industry experience is preferred.
- R programming and safety experience are specifically required.
- SAS knowledge is preferred for Clinical Programming.
- Python and other relevant programming languages may also be applicable.
- Knowledge of ICH-GCP and clinical research concepts is required.
- The role can involve CDISC-compliant data packages and submission support.
- Application deadline: October 14, 2026.
- Salary/CTC is not specified in the supplied vacancy.
Frequently Asked Questions
1. What is the job title at Johnson & Johnson?
The position is Experienced I Statistical Programmer.
2. Where is this job available?
The position is listed for Bangalore, Mumbai, and Hyderabad.
3. Is this a remote job?
No. The vacancy specifies a hybrid work model.
4. How much experience is required?
The posting mentions approximately 2+ years of relevant programming experience.
5. Which programming language is specifically required?
The vacancy specifically highlights R language and safety experience as required.
6. Is SAS knowledge required?
SAS knowledge is listed as preferred for the Clinical Programming role.
7. Can Python experience be relevant?
Yes. The vacancy identifies SAS, R, Python, and other relevant programming languages as possible tools for data manipulation, statistical analysis, and reporting.
8. What educational qualification is required?
A Bachelor’s degree or higher, or equivalent technical/theoretical depth, in Computer Science, Data Science, Data Engineering, Mathematics, Public Health, or another relevant scientific field is specified.
9. Does the role involve clinical trials?
Yes. The position supports programming, data analysis, reporting, and submission activities associated with clinical trials.
10. Does the role involve CDISC?
Yes. The position may support creation, verification, and delivery of CDISC-compliant data packages and reviewer’s guides.
11. What is the application deadline?
The stated deadline is October 14, 2026.
12. What is the requisition ID?
The job requisition ID is R-074782.
13. Is salary mentioned?
No. The supplied job posting does not specify a salary or CTC.
Important Note
Job availability, eligibility requirements, application deadlines, work locations, and recruitment conditions may change. Candidates should verify the latest information on the official Johnson & Johnson careers portal before applying. Meeting the listed requirements does not guarantee selection or employment.