Teams at Syneos Health

Support design and execution of retrospective and prospective real-world evidence studies, conduct literature reviews and qualitative research, analyze and interpret real-world data, develop protocols, reports, manuscripts, and client presentations, and use Microsoft Office and statistical software to produce high-quality deliverables under senior guidance.

Lead statistical programmer developing SAS code and ADaM-specified datasets, tables, listings, and graphs for clinical trials. Ensures quality, validation, documentation, inspection readiness, mentors programmers, manages timelines, participates in sponsor meetings, and follows regulatory and SOP requirements.

Lead operational execution of a complex Phase 2b inflammation trial from start-up through closeout. Independently manage day-to-day study operations, timelines, risks, vendor/CRO oversight, cross-functional leadership, study documentation, budget tracking, and training. Drive issue resolution, mentor junior staff, and implement process improvements in a sponsor-dedicated, fast-paced environment.