Related skills
r git sas cdisc sdtm📋 Description
- Develop, validate, and maintain SDTM and ADaM datasets using R per CDISC standards.
- Support TLF (Tables, Listings, Figures) generation in R or SAS as needed.
- Write efficient, reproducible R scripts for clinical data analysis and reporting.
- Collaborate with biostatistics, data managers, and clinical teams to gather programming requirements.
- Ensure regulatory deliverables meet FDA/EMA expectations.
- Contribute to programming workflows and version control practices.
🎯 Requirements
- Bachelor's or Master's in Statistics, CS, Math, Life Sciences, or related field.
- 4-6+ years in clinical programming with strong R focus.
- Proven SDTM and ADaM dataset creation using R.
- Working knowledge of SAS programming.
- Solid CDISC SDTM/ADaM understanding.
- Experience in CRO/pharma environment.
- Strong analytical, problem-solving, and documentation skills.
- Preferred: tidyverse, haven, pharmaverse (admiral, tidyCDISC).
🎁 Benefits
- Remote work opportunity
- Global CRO with career growth
- Equal opportunity employer, diverse teams
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