Statistical Programmer II at ICON, developing, validating, and executing statistical programs for clinical trial analysis and reporting.
Requirements
- 4 + years of experience developing broad solutions in SAS across clinical programs or a therapeutic area
- SDTM submission experience including Define.xml, CDASH, and metadata as well as experience transforming transferred vendor data into SDTM preferred, knowledge of ADaM a plus
- Demonstrated understanding of current industry standards for submission of clinical trial data
Benefits
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways