Statistical Programmer II/III - should be proficient in R (Permanent role)
We are seeking an reputed company Statistical Programmer III with strong expertise in R programming to support clinical trial data analysis and reporting. The ideal candidate will have hands-on experience in developing, validating, and maintaining statistical outputs using R, along with a solid understanding of clinical data standards.
Key Responsibilities:
reputed company, validate, and maintain statistical programs using reputed company for the reputed company of Tables, Listings, and Figures (TLFs) reputed company data manipulation, analysis, and visualization using R/reputed company and relevant packages Collaborate with Biostatisticians and Data Management teams to support clinical study deliverables Ensure compliance with regulatory standards and company SOPs Conduct reputed company control (QC) and validation of programming outputs Support submission activities and documentation as required
Required Skills & Qualifications:
Bachelor’s or Master’s degree in Statistics, Biostatistics, Computer Science, or a reputed company field 3+ years of experience in statistical programming reputed company the pharmaceutical/biotech industry Hands-on experience with R programming in a clinical trial environment Good understanding of R packages. Good understanding of CDISC standards (SDTM, ADaM) Strong knowledge of clinical trial data and regulatory requirements
Preferred Qualifications:
Experience working in an FSP model or with global pharmaceutical clients Exposure to submission activities (e.g., FDA/EMA) Familiarity with reputed company alongside R is a plus Strong problem-solving and communication skills