Lead Programmer

Job highlights

• Bachelors or Masters degree in Computer Science,Statistics,Mathematics,Life Sciences,or related field. . 6+ years of experience in clinical programming within pharmaceutical,biotechnology,or contract research organizations. . Strong proficiency in SAS programming and experience with clinical data standards such as SDTM (Study Data Tabulation Model).

Job Summary

Position Summary Join us as a Lead Programmer and take the lead in delivering high-quality programming solutions that support innovative healthcare research. In this role, you will collaborate closely with scientists, data managers, and project teams to turn complex data into meaningful insights. Your expertise will help our teams progress efficiently while ensuring compliance and data integrity. We value candidates who are proactive, skilled communicators, and eager to grow in a supportive and inclusive environment. At GSK, you will have the chance to develop your career while making a real impact on health through science and technology.

Responsibilities

• Lead the development, validation, and review of programming deliverables for clinical trial data conversion and analysis.
• Guide the creation and validation of study-specific and standard programs using SAS and other programming languages.
• Manage end-to-end study programming activities, ensuring timelines and quality standards are met.
• Support and mentor programming team members, providing guidance on troubleshooting and best practices.
• Collaborate with cross-functional teams to gather requirements and deliver on study-specific programming needs.
• Maintain adherence to relevant processes, regulations, and industry standards while promoting data integrity.

Requirements

• Bachelor's or Master's degree in Computer Science, Statistics, Mathematics, Life Sciences, or related field.
• 6+ years of experience in clinical programming within pharmaceutical, biotechnology, or contract research organizations.
• Strong proficiency in SAS programming and experience with clinical data standards such as SDTM (Study Data Tabulation Model).
• Proven experience in developing, validating, and reviewing clinical trial programming deliverables.
• Experience managing or leading programming projects or teams.
• Good understanding of regulatory requirements and industry best practices related to clinical data.

Qualifications

• Experience with additional programming languages such as R or Python.
• Familiarity with ADaM (Analysis Data Model) and TLF (Tables, Listings, and Figures) programming.
• Knowledge of data visualization and reporting tools like Spotfire or similar.
• Experience in implementing defensive programming techniques or automation in programming workflows.
• Strong communication and interpersonal skills with the ability to engage stakeholders effectively.
• Previous experience working in a hybrid work model; this role is based in Bengaluru with hybrid working (3-4 days in office).

Skills

• Agile Thinking
• Clinical Data Management
• Data Analysis
• Data Visualization
• Learning Agility
• Pharmaceutical Industry
• Stakeholder Management
• Statistical Analysis

Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.