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As a Senior Statistical Programmer I, you will develop and validate SAS programs for clinical trial data analysis, collaborate with biostatisticians, and ensure compliance for high-quality results and reporting.

As a Study Start Up Associate II, you will lead regulatory document preparation, coordinate stakeholder approvals, maintain accurate records, and support study teams in compliance and best practices.

Manage full lifecycle of grants, donations, sponsorships and exhibits for Global Medical Affairs: review requests, oversee committee meetings, contracting, budget tracking, payments, reconciliations, reporting, data systems, and cross‑functional compliance communications.

The role involves providing DMPK expertise, conducting reviews of nonclinical programs, preparing regulatory submissions, and engaging in business development initiatives.