Related skills
r sas cdisc sdtm adam📋 Description
- Program for clinical trials: derive datasets, tables, figures, listings.
- Process data from external sources and support publications.
- Perform ad hoc exploratory analyses for publications.
- Oversee programming deliverables from CROs.
- Contribute to CRF, Data Transfer, SAP, and SDTM/ADaM specs.
- Electronic submissions: CDISC compliant deliveries.
🎯 Requirements
- Bachelor or Master in CS, Math, Engineering, Medical, or related field.
- BS+5 yrs or MS+3 yrs in statistical programming (SAS, R) in pharma.
- Working knowledge of SAS and its components.
- Knowledge of R programming in clinical trials.
- Strong SAS and SAS Macro language skills.
- Ability to work on data integrations (ISS and ISE).
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