Related skills
r sas clinical trials statistical programming cdisc📋 Description
- Program and validate derived datasets, tables, listings.
- Perform ad hoc exploratory analyses for publications.
- Oversee programming deliverables from CROs and vendors.
- Contribute to design/implementation of CRF, SDTM/ADaM documentation.
- CDISC submissions: program and validate deliveries.
- Project management: ensure on-time, high-quality deliverables.
🎯 Requirements
- Bachelor or Master in CS, Math, Engineering, Medical or related.
- BS+5y or MS+3y in statistical programming (SAS, R) in pharma.
- Working knowledge of SAS and its components.
- R programming in clinical trials.
- Strong SAS and SAS Macro language skills.
- Familiarity with the drug development process.
🎁 Benefits
- Equal opportunity employer.
- Focus on professional development and training.
- Global CRO with diverse, client-facing teams.
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