Key Roles & ResponsibilitiesResponsible for clinical development strategies, including Phase I through III in oncology, life cycle management, safety responsibilities, scientific interactions with regulatory authorities, internal cross functions and external partners.

Leads and oversees the strategic definition and tactical development of clinical trials programs, including protocol, interpretation of clinical data, and literature reviews.

Accountable for the delivery of projects according to quality, time, budgets, and resourcesEnsures that clinical trials are conducted in accordance with applicable regulatory requirements and guidelines.

Play a lead role in the development and implementation of communications strategies to support existing and completed studies including KOL interactions, advisory boards, major medical meetings, congresses and other events, publications and other materials.

Contribute clinical science input into the relevant therapeutic/disease area scientific strategy.

Identify strategic and incremental organizational resource needs re: People, Process and Technology.

Plan and direct career development for China & US oncology team members.