Manage cross-functional teams to define and implement nonclinical drug safety strategies in immunology and oncology, ensuring the successful transition of drug candidates from discovery to regulatory approval. Emphasize risk assessment and innovative solutions.

Optimize late-stage clinical drug development by leading statistical programming, ensuring timely delivery of analysis, and collaborating with stakeholders to drive quality in regulatory submissions and project execution.

Drive transformational impact by applying mechanistic modeling and numerical simulation to downstream biologics processes, influencing purification decisions and mentoring team members in a collaborative, innovative environment.

Empower drug discovery by leading strategic nonclinical safety initiatives across therapeutic areas, ensuring optimal risk assessment and collaboration to support innovative medicines that enhance patient care.

Drive innovative drug discovery by leading nonclinical safety strategies across therapeutic areas while collaborating with cross-functional teams to evaluate therapeutic targets and develop new drug candidates for patients in need.