Experienced Clinical Programmer I

About the organization

Johnson & Johnson Innovative Medicine is focused on discovering, developing, and bringing to market advanced medicines. Its work spans oncology, immunology, neuroscience, cardiovascular conditions, and metabolic disorders, with an emphasis on science-led, patient-focused healthcare innovation.

The company is committed to building an inclusive workplace where people are treated with respect, valued for their individuality, and recognized for their contributions.

Role overview

This position is part of the Data Analytics / Computational Sciences function, specifically within Biostatistics. The Clinical Programmer acts as an individual contributor with working knowledge of data structures, programming standards, and programming methods. The role supports analysis and reporting activities for clinical trials in line with internal processes and procedures.

The role is expected to support one or more trials with low to medium complexity or criticality and may also take part in innovation and process-improvement initiatives within the department.

What you'll do

• Deliver programming support for trial activities of low to medium complexity with strong quality and turnaround discipline, and take the lead where needed.
• Build and maintain programs that support clinical research analysis and reporting.
• Check programming outputs and reporting work to an appropriate level and review project requirements and supporting documentation.
• Contribute to submission-related work, including the preparation, validation, and handoff of CDISC-compliant or non-standard datasets and reviewer guides.
• Follow department procedures, apply the latest standards, and use current technologies in day-to-day work.
• Participate in departmental innovation and operational improvement initiatives when assigned.
• Work closely with team members and cross-functional stakeholders.
• Stay compliant with required training, time entry, and other operational expectations.
• Review specifications for mapping the internal Data Review Model (DRM) to ensure it is suitable for reporting use and properly verified.
• Support data-cleaning efforts by creating edit checks and review listings, and assist with reporting through visualizations and listings for data management, medical monitoring, and central monitoring.

Collaboration and reporting structure

The role reports to a people manager within the Delivery Unit and is accountable to Portfolio and Study Leads for assigned work. It interacts with internal teams such as Data Management, Central Monitoring, Programming, Clinical Data Standards, Regulatory Medical Writing, and system support groups, as well as broader functions including Statistics, Clinical, Global Medical Safety, Project Management, Regulatory, Strategic Partnerships, and Human Resources. External interaction may include partners, CRO management, vendor contacts, and industry working groups.

Qualifications and experience

A bachelor’s degree or higher is expected, or an equivalent level of technical depth, in computer science, data science, data engineering, mathematics, public health, or another relevant scientific discipline.

Applicants should have about 2+ years of relevant programming experience, ideally in pharmaceuticals, CROs, biotech, or a related industry. A basic understanding of regulatory guidance such as ICH-GCP and relevant clinical research and development concepts is needed. Experience working in a team environment is preferred, along with strong written and verbal communication skills.

Candidates should understand data structures and programming languages used for data manipulation, statistical analysis, and reporting, such as SAS, R, and Python. For this role, SAS experience is preferred. A working knowledge of programming methods, processes, and concepts used in clinical programming is also important.

The role also calls for working knowledge of clinical programming tools and languages such as SAS and SQL, along with a willingness to keep learning and adapt to next-generation data strategy tools such as Python.

Eligibility

Any graduate may apply, provided they meet the role’s educational and experience expectations.

Additional information

All listed locations for this posting are Bangalore, Karnataka, India; Mumbai, India; and Penjerla, Telangana, India. This posting includes a general disclaimer that the role details, content, and availability may change, and candidates should verify the latest information directly with the employer before proceeding.