Senior Statistical Programmer
IQVIA (company site, opens in a new tab)HyderabadOn-siteDirect career pageEst. 18–30 LPA
Posted 7h ago
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Job description
Structured overview of role & requirements
About This Role
- Develop and validate R packages and R-Shiny applications for clinical trial analysis and decision-making.
- Conduct statistical programming and validation of safety and efficacy outputs (ADaM, TLFs) aligned with protocols and standards.
- Lead R implementation efforts and support/train Biostatistics team members in statistical programming.
Minimum Requirements
- Strong hands-on programming skills in R and R-Shiny, with ability to reproduce statistical analyses.
- Advanced knowledge of CDISC standards (SDTM/ADaM) and standard program development practices.
- Prior Data Scientist experience applying programming skills in clinical or broader data science contexts.
- Work Experience Required: Not explicitly mentioned in the JD
Ideal Candidate Profile
- Experience with clinical trial statistical methodologies and late-phase, Real-World Evidence (RWE), or Global Medical Affairs studies.
- Operational experience leading R programming efforts and enabling team capabilities through support and training.
- Skillful in data visualization and data wrangling with R, indicating an analytical and solution-oriented approach.