Associate Medical Affairs Director

Major Responsibilities：

• Drive pipeline local development and brand LCM strategy
• Provide broad and deep understanding of the therapeutic area. Seen as cred-ible medical and scientific expert by internal and external customers.
• Contribute strategic, medical, clinical and scientific guidance to all allied de-partments in OBU China, including support the local GMO team for timely ex-ecution of studies conducted in China and to DRA in interactions with authorities
• Drive collaboration of  Medical Advisors team with other business function teams in China, Regional and Global in the execution of relevant clinical activities including initial input in programs strategy and designs of clinical studies.
• May serve as CPO/EGM representative on Global Teams, as assigned (as a potential member of the GPT).
• Oversee design, conduct and quality of post  marketing trials including profil-ing programs.
• Oversee together with IMS local clinical trial adverse event reporting as well as clinical input and oversight into adherence to GCP together with GMO head.
• Collaborate actively with Marketing partners to ensure  development and im-plementation of C4MPH.
• Lead the development of Medical Plan.
• In collaboration with GMO, advise / recommend potential investigators for local and global studies, ensuring the right mix of KOLs.
• Coach and provide guidance to the staff to be compliant

Requirement：

• MD degree in oncology
• Fluent in English (oral and written)
• Typically would have more than 5 years of managerial expe-rience in the pharmaceutical industry with focus on oncology.
• State-of-the-art medical, scientific and clinical knowledge.
• Proven ability to lead and coach scientific/medical personnel at all skill and knowledge levels.
• Strong interpersonal, communication, negotiation, and presen-tation skills.
• Professional respect and credibility with extensive knowledge of therapeutic area, encompassing business strategy and mar-ket trends.
• Familiar with respective health authority, GCP and ICH re-quirements, including regulations of Promotional materials.
• Expert in all aspects of clinical drug development including experience designing and/or executing clinical studies to ad-dress local BF/BU needs.
• Successful development and implementation of innovative programs and processes.
• Pronounced interest in commercial success of projects/products in oncology.
• Strong knowledge of the market preparation and access re-quirements, encompassing medical strategies and market trends.