Ephicacy
Website:
ephicacy.com
Job details:
Develop and validate R programs for analysis datasets and Tables, Listings & Figures (TLFs)
- Support Phase I–IV clinical trials across efficacy, safety, and exploratory analyses
- Create reusable R packages and automated reporting solutions using the pharmaverse ecosystem
- Develop CDISC-compliant SDTM and ADaM analysis datasets
- Deliver submission-ready outputs for FDA, EMA, PMDA, and other global regulatory agencies
- Collaborate with statisticians to implement Statistical Analysis Plans (SAPs)
- Drive programming quality through independent QC, validation, and adherence to industry standards
Required Skills:
7+ years of Clinical Statistical Programming experience
✅ 3–5+ years of hands-on R programming in the Pharmaceutical, Biotechnology, or CRO industry
✅ Strong expertise in:
- R Programming
- CDISC SDTM & ADaM
- TLF Generation
- SAP Implementation
- Clinical Trial Reporting
Click on Apply to know more.