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Johnson & Johnson is a global healthcare company working across innovative medicine and medical technology. Its teams develop solutions in oncology, immunology, neuroscience, specialty ophthalmology, interventional care, and orthopaedics, combining science and technology to address complex health needs. The company also emphasizes health equity, environmental sustainability, diversity, and inclusion as it serves providers, patients, and communities worldwide.
Statistical Programmer, Clinical Research - Johnson & Johnson, Bangalore Hybrid
Support clinical trial programming, analyses, and CDISC-compliant submissions for Johnson & Johnson’s healthcare research programs. Develop R-based safety and reporting solutions while contributing to reliable clinical data deliverables.
Description
- Program and, where appropriate, lead low- to medium-complexity clinical trial activities while delivering accurate work on schedule.
- Create and maintain programs for clinical research analyses and reporting.
- Verify programming outputs and reporting activities using appropriate quality checks.
- Review project requirements and contribute to supporting documentation.
- Help prepare, verify, and deliver CDISC-compliant and non-standard data packages and reviewer guides for submissions.
- Apply departmental procedures, current standards, and up-to-date technologies in daily programming work.
- Participate in innovation initiatives and projects that improve departmental processes.
- Work effectively with team members and cross-functional colleagues.
- Complete required training, time reporting, and other company and departmental operational processes.
- Report to a Delivery Unit people manager and remain accountable to Portfolio and Study Leads.
- Coordinate with internal functional teams, external partners, CRO management, vendor liaisons, industry peers, and working groups.
Requirements
- Bachelor’s degree or higher, or equivalent expertise, in computer science, data science or engineering, mathematics, public health, or another relevant scientific discipline.
- About two or more years of relevant programming experience, preferably in pharmaceuticals, CROs, biotechnology, or a related industry.
- Basic familiarity with regulatory guidance such as ICH-GCP and with clinical research and development concepts.
- Experience working collaboratively in a team setting is preferred.
- Strong written and verbal communication skills.
- Knowledge of data structures and programming languages used for data manipulation, statistical analysis, and reporting, including SAS, R, or Python.
- Basic understanding of programming processes, methods, and concepts.
- Experience with the R language and safety programming.
- SAS knowledge is preferred for clinical programming work.
Benefits
- An inclusive workplace environment.
- A culture that respects employee diversity and dignity.
- Recognition for employee merit.
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