Provide medical leadership for oncology drug development programs from preclinical development through clinical stages.
Lead and/or contribute to the development of clinical translation strategies, clinical development plans, and target product profiles.
Author and review of study protocols, investigator brochures, safety and medical monitoring plans, and regulatory documents.
Provide input into regulatory interactions, IND-enabling activities, and clinical trial design and execution.
Serve as the medical lead to cross-functional project teams.