Novartis is seeking a Senior Statistical Programmer responsible for leading statistical programming activities for clinical studies, ensuring timely and high-quality deliverables. The ideal candidate will have substantial experience in programming with R or SAS, knowledge of CDISC standards, and the ability to collaborate effectively with cross-functional teams
Job Summary
The Senior Statistical Programmer leads statistical programming activities for Phase I–IV studies to ensure efficient execution of pharmaceutical drug-development plans.
Candidates must possess expert-level skills in R or SAS with at least five years of practical experience in clinical trial programming.
Novartis offers a collaborative community environment where smart, passionate people work together to create breakthroughs that change patients' lives.
Matching Summary
Match Score: 85
Novartis is seeking a Senior Statistical Programmer responsible for leading statistical programming activities for clinical studies, ensuring timely and high-quality deliverables. The ideal candidate will have substantial experience in programming with R or SAS, knowledge of CDISC standards, and the ability to collaborate effectively with cross-functional teams.
Skills & Requirements
Must-have
Expert R or SAS programming skills
5+ years clinical trial programming experience
Independent SDTM/ADaM design and implementation
PMDA E-data submission experience
Team lead experience for programming projects
Nice-to-have
R package development capabilities
Python or other language proficiency
Project management and resource scheduling
Tool development for process optimization
Post-marketing surveillance (PMS) experience
Key Requirements
BA/BS/MS in statistics, computer science, or related field
Minimum 5 years of clinical trial programming experience
Fluency in Japanese and English communication
Experience leading programming teams as a Trial programmer or CRO lead