Statistical Programmer
2 weeks ago
Location: Bangalore (Remote)
Experience:6+ years as a Statistical Programmer, with minimum 1 year in R programming
Work Mode: Full-time, Remote
Job Description:
We are seeking an experienced Senior/Principal Statistical Programmer with expertise in R programming for clinical trial data analysis. The ideal candidate will have strong statistical programming skills and experience working with regulatory submissions.
Key Responsibilities:
Develop, validate, and maintain statistical programs using R for clinical trial data analysis.
Generate Tables, Listings, and Figures (TLFs) for regulatory submissions.
Work on CDISC standards (SDTM/ADaM) for data analysis and reporting.
Collaborate with biostatisticians and clinical teams to ensure high-quality statistical deliverables.
Perform quality checks and validation of programming outputs.
Adhere to regulatory guidelines (FDA, EMA) and industry standards.
Required Skills:
6+ years of experience as a Statistical Programmer.
Minimum 1 year of experience in R programming.
Strong understanding of clinical trial data and regulatory guidelines.
Experience with CDISC SDTM/ADaM standards.
Excellent problem-solving and communication skills.
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