Teams at Syneos Health

Provide statistical programming support for clinical studies, collaborating with statisticians and project teams to produce analysis datasets, tables, listings, and figures; ensure quality, regulatory compliance, and timely delivery for clinical development programs.

Lead statistical programming for clinical trials using SAS to produce ADaM datasets, summary tables, listings, and figures (TLFs). Develop and validate code, maintain documentation, review statistical specs, mentor programmers, manage multiple projects, ensure regulatory compliance, and participate in sponsor meetings. Minimal travel may be required.

The Safety & PV Specialist I is responsible for data entry and tracking of safety reports, maintaining compliance with SOPs, and conducting literature reviews related to safety in clinical trials.