Senior Clinical Programmer II

Overview

As a Senior Clinical Programmer II, you will lead clinical programming and data visualization that support trial oversight, data cleaning, reporting, and evidence-based decisions across global studies. You will develop validated listings, dashboards, and analytical solutions; shape programming standards; manage quality and risk; and mentor junior programmers.

What you'll do

• Independently design, develop, implement, and validate complex programs in SAS, Python, R, SQL, Power BI, Spotfire, and other dashboard technologies.
• Deliver efficient code that processes, analyzes, and reports clinical trial data for timely review by study teams.
• Build and maintain dashboards and data visualization tools end to end, including requirements gathering, data provisioning, development, and optimization.
• Create and maintain a catalogue of listings and reports for systematic data cleaning and issue detection.
• Lead small to medium complexity initiatives aligned to the clinical programming roadmap.
• Define and contribute to processes, reusable components, and best of the industry practices for programming deliverables.
• Build quality into outputs, review deliverables from other programmers, and identify, manage, and communicate risks and mitigation plans.
• Serve as a subject matter authority on programming topics and collaborate with data management, development operations, clinical, biometrics, and other teams.
• Mentor and coach junior programmers and provide cross-training, technical guidance, and support for reports and dashboards.
• Oversee complete and accurate documentation of programming activities in adherence to standard operating procedures, guidelines, and best of industry practices.

What you'll need

• Bachelor’s/Master’s degree or equivalent in computer science, life science, or statistics.
• Accomplished programming skills in SAS, Python, R, SQL, Power BI, SpotFire, or other dashboard technologies.
• Proficient knowledge of the clinical development process.
• Thorough knowledge of industry standards.
• Ability to influence relevant collaborators.
• Excellent analytical and critical thinking skills, writing and communication skills, and ability to work within a cross-functional team.
• Excellent collaborative skills and the ability to handle complexity and change in a dynamic environment.
• Technical expertise with data capture, data models, data mining, and visualization techniques.
• Prior experience and understanding of EDC systems like Medidata Rave, Inform, and Veeva and data platforms like Saama, Entimice, and SAS LSAF.

Nice to have

• Strong interpersonal abilities and the capacity to navigate complexity and adapt to change in a fast-paced environment.
• Broad knowledge of FDA regulations and GCP/ICH guidelines as related to clinical programming processes.
• Experience producing analytical dashboards with Power BI, Spotfire, or alternative Business Intelligence platforms.
• Knowledge of MicroStrategy.

Details

• Location: Manyata Tech Park, Bangalore, India.
• Work type: Hybrid.
• In-person working is expected, on average, a minimum of three days per week from the office.
• Role type: Individual Contributor.