Develop, validate, and maintain SAS programs for study data analysis and reporting
Create datasets, tables, listings, and figures per study requirements
Collaborate with Biostatistics, Data Management, and Clinical teams
Ensure programming deliverables meet quality standards and timelines
Participate in study planning, review specs, and support submissions

🎯 Requirements

Strong SAS programming experience in pharma/CRO
Hands-on CVRM studies experience
Experience generating/validating SDTM, ADaM, and TLFs
Knowledge of CDISC standards and trial processes
Ability to work independently and manage multiple priorities
Experience supporting regulatory submissions is preferred
Strong communication and stakeholder management

🎁 Benefits

Professional development opportunities
Supportive culture and client-facing work

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