Overview
Lead clinical programming and data visualization for global clinical studies, turning trial data into validated reports, dashboards, and analytical insights. The role also includes quality oversight, cross-functional collaboration, and mentoring junior programmers.
What you'll do
- Design, develop, implement, and validate complex clinical-programming solutions.
- Build and maintain dashboards and visualization tools for data quality, safety, and operational monitoring.
- Create listings and reports to support data cleaning and issue detection.
- Lead small- to medium-complexity initiatives aligned with the clinical programming roadmap.
- Define reusable processes, tools, and programming best practices.
- Review deliverables, manage risks, and communicate mitigation plans.
- Mentor junior programmers and oversee programming documentation.
What you'll need
- Bachelor’s or master’s degree in computer science, life science, statistics, or an equivalent qualification.
- Strong programming skills in SAS, Python, R, and SQL.
- Experience with Power BI, Spotfire, or other dashboard technologies.
- Proficient knowledge of the clinical development process.
- Thorough knowledge of industry standards.
- Experience with clinical data capture, data models, data mining, and visualization techniques.
- Experience with EDC systems such as Medidata Rave, Inform, or Veeva, and data platforms such as Saama, Entimice, or SAS LSAF.
Nice to have
- Knowledge of FDA regulations and GCP/ICH guidelines related to clinical programming.
- Experience producing analytical dashboards with Power BI, Spotfire, or alternative business intelligence platforms.
- Knowledge of MicroStrategy.
Details
- Location: Bangalore, Karnataka, India.
- Work mode: Hybrid, with an average minimum of three office days per week.
- Role type: Individual Contributor.
Read the full description and apply on the company’s own careers page.
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