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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.

The Director of Safety Science will lead safety strategy for clinical programs, oversee adverse event reporting, and manage pharmacovigilance governance, while collaborating across departments to ensure patient safety and compliance.

Lead clinical data management across multiple trials, set strategy and standards, oversee CROs/vendors, ensure analysis-ready and regulatory-compliant data, manage EDC systems and key deliverables (DMPs, CRFs, edit checks, database locks), mentor team, and collaborate with Biostatistics, Clinical Operations, and Regulatory Affairs.

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.