Senior Clinical Programmer II
AstraZeneca (company site, opens in a new tab)BengaluruOn-siteDirect career pageEst. 18–30 LPA
Posted 10h ago
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Job description
Structured overview of role & requirements
About This Role
- Lead design, development, and validation of complex clinical programming outputs using SAS, Python, R, SQL, and dashboard tools to analyze clinical trial data.
- Build and maintain dashboards and reports that enable data quality monitoring, safety tracking, operational performance, and systematic data cleaning for global clinical studies.
- Drive project initiatives aligned with clinical programming roadmap, define standards and best practices, manage quality and risks, and mentor junior programmers.
Minimum Requirements
- Bachelor’s or Master’s degree in computer science, life science, or statistics.
- Strong programming skills in SAS, Python, R, SQL, and proficiency with data visualization tools such as Power BI or Spotfire.
- Proficient knowledge of clinical development processes and industry standards including experience with EDC systems (Medidata Rave / Inform / Veeva) and data platforms (Saama, Entimice, SAS LSAF).
- Work Experience Required: Not explicitly mentioned in the JD.
Ideal Candidate Profile
- Experienced in independently delivering end-to-end clinical programming solutions impacting global studies with attention to quality and compliance.
- Capable of influencing cross-functional teams including data management, clinical, and biometrics, with deep understanding of clinical data and regulatory standards.
- Demonstrates leadership in mentoring others, advancing enterprise programming standards, and leveraging digital tools to accelerate clinical data insights.