**GCF D7 for Oncology TA Lead**


+ Accountable for determining and evaluating medical, scientific & clinical strategies both near and long term for the TA

+ Drive the planning processes, data generation, establishing and communicating the medical strategy for the China TA

+ Provide local medical landscape section in support of Regulatory filing for clinical trial application, and China participation of global clinical study

+ Leading the China Oncology TA Network and, where necessary, supports the countries in navigating products through internal and external governance and regulatory portals

+ Provide local medical input on treatment paradigm, guidance, unmet need for the global team in the product development and study design for global and China.

+ Responsible for data review and participates in KOL/Trial speaker development

+ Supports regulatory and ethics approvals for China local trials

+ Engages with relevant individuals including thought leaders, institutions and societies to generate medical insight.

+ Organizes and/or conducts Medical Advisory Boards Meetings/Expert Panels and participates in Investigator Meetings

+ Managing resources and budget for the TA

+ Coaching, mentoring and developing staff and team members

**Key Qualification and Capabilities**

+ Medical Doctor

+ 3 years or more clinical practice experiences

+ 5 or more years of clinical research experience in the biopharmaceutical industry (biotech, pharmaceutical) or significant interest in one or more of the following therapeutic areas: lipidology, cardiovascular disease, diabetes

+ Experience with clinical study management and conduct

+ Experience with scientific expert interactions

+ Fluency in English, both oral and written communications

+ Familiarity with concepts of clinical research and clinical trial design, including biostatistics

+ Knowledge of Good Clinical Practices (GCP), FDA, EMEA/CHMP and CFDA regulations and guidelines, and applicable international regulatory requirements

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