PROGRAMMING MANAGER
GSK (company site, opens in a new tab)5+ yrsBengaluruOn-siteDirect career pageEst. 18–28 LPA
Posted 11h ago
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Job description
Structured overview of role & requirements
About This Role
- Lead clinical programming activities for multiple studies, delivering high-quality datasets, tables, listings, and figures.
- Provide technical leadership and oversight for outsourced programming teams and external vendors to ensure regulatory readiness and quality.
- Define, implement, and maintain programming standards, review study documents, manage risks, and mentor programming team members.
Minimum Requirements
- Bachelor’s degree in computer science, statistics, mathematics, life sciences, or related field.
- Minimum 5 years of clinical or statistical programming experience supporting clinical trials.
- Strong SAS programming skills including macro development and reusable code.
- Practical understanding of clinical data standards (SDTM, ADaM) and experience managing programming deliverables and oversight of vendors.
Ideal Candidate Profile
- Experienced in clinical trial programming with hands-on SAS and familiarity with clinical data standards and submission processes.
- Capable of technical leadership and managing outsourced vendors while improving programming processes and templates.
- Proven mentor and collaborator comfortable with cross-functional teams and communicating with both technical and non-technical stakeholders.