Lead talent acquisition and HR strategies for organizational growth, partnering with leadership to manage hiring processes and ensure alignment with clinical development milestones.

Lead statistical programming strategy and execution across clinical studies, ensuring regulatory-compliant outputs (SDTM, ADaM, TLFs). Oversee SAS development, validation, infrastructure, automation, and vendor management while partnering with Biostatistics, CDM, Regulatory Affairs, and IT to deliver reproducible, submission-ready deliverables.

The Director of Biostatistics leads statistical strategy for clinical studies, ensuring robust execution, regulatory compliance, and collaboration with cross-functional teams. Responsibilities include overseeing technical activities, managing CROs, and influencing study design and submissions.