Champion supply chain strategy and execution for clinical operations, ensuring timely, compliant delivery of materials for global oncology trials. Collaborate with cross-functional teams to manage risks and optimize supply models while driving success.

Lead cutting-edge oncology clinical studies focusing on FIH and Phase 1 trials. Collaborate with multidisciplinary teams to design and implement protocols, ensuring compliance and advancing innovative cancer therapies for patient benefit.

Empower teams in analytical development and quality control to ensure compliance and operational efficiency. Collaborate closely with cross-functional groups to advance clinical asset goals and support regulatory submissions.

Develop and oversee clinical pharmacology strategies across stages of drug development. Drive modeling efforts and regulatory submissions, ensuring communication with stakeholders while guiding pediatric study designs and analyses.

Explore impactful opportunities as you engage healthcare professionals, foster relationships, and provide valuable medical insights, driving patient care forward in a dynamic, field-based environment where your expertise shapes medical strategy.