Lead Programmer
GSK (company site, opens in a new tab)6+ yrsBengaluruOn-siteDirect career pageEst. 18–35 LPA
Posted 8h ago
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Job description
Structured overview of role & requirements
About This Role
- Lead the development, validation, and review of clinical trial programming deliverables, ensuring quality and timelines are met.
- Manage end-to-end study programming activities and mentor team members on troubleshooting and best practices.
- Collaborate with cross-functional teams to gather requirements and ensure adherence to regulatory and industry standards for data integrity.
Minimum Requirements
- Bachelor’s or Master’s degree in Computer Science, Statistics, Mathematics, Life Sciences, or related field.
- 6+ years of clinical programming experience in pharmaceutical, biotechnology, or contract research organizations.
- Strong proficiency in SAS programming and experience with clinical data standards such as SDTM.
- Work Location: Bengaluru with hybrid work model (3-4 days in office).
Ideal Candidate Profile
- Experienced clinical programmer with leadership or project management experience in clinical trial programming.
- Proficient with regulatory requirements and industry best practices related to clinical data handling.
- Familiarity with multiple programming languages (e.g., SAS, R, Python) and advanced clinical data models (e.g., ADaM) preferred.