Medical Affairs Manager, Solid Tumour

Major Responsibilities：

• Contribute to C4MPH/LRR strategy and its alignment of assigned products/disease areas. Develop tactical plans within phase IV budgets.
• As a “Medical Champion”, lead China Program Team (CPT) for responsible products/disease areas to drive brand LCM and pipeline development strategy.
• Provide strategic, medical, clinical and scientific guidance to allied peers in departments in OBU China, including Medical Sientific Liaisons (MSL), Integrate Medical Safety(IMS), Medical Information Service (MIS) and Clinical Operations (GMO)
• Cooperate with Drug Regulatory Affairs (DRA) on clinical dossier preparation and interactions with authorities to ensure success of IND/NDA filing & approval.
• Lead local Advisory Board meetings for LCM, pipeline development strat-egy and protocol discussion for responsible products/disease areas in line with global/EGM therapeutic medical leaders
• Define, plan, initiate and manage local clinical trials including local regis-tration trials, PMS studies and LCM related third party studies in line with GCP, local regulations and NVS standards.
• Provide medical support to the local GMO team for timely execution and scientific quality of NVS sponsored studies including global and local tri-als
• Provide medical insight to medical marketing activities (e.g. Advisory Board meetings, promotional materials, scientific slides deck, publications) on key scientific messages for assigned product(s)/disease areas.
• Responsible for MCC review for assigned product(s)/disease areas and ensure the scientific quality.
• Provide comprehensive Disease/Therapy/Product presentations and training to internal and external customers, including clinical GMO team, DRA team and the field force if required in line with C4 MPH plans.
• Maintain top KOL management and strong relationship with scientific as-sociations jointly with marketing, GMO team
• From medical strategy perspective, provide insight to Managers and MSLs for proactive data dissemination to reinforce clinical awareness, and develop and maintain the support of KOLs, influencers and key external stakeholders.
• Ensures materials distributed internally or externally are fully align with NP4/G3 guidelines from scientific point of View.
• Coach and provide guidance to the staff to be compliant:

Requirement：

• 5+ years of clinical research experience/pharmaceutical industry experience required and managerial experience preferred
• Advanced medical/scientific writing and communication skills
• Proven ability to design, interpret, discuss and represent clinical trial data and establish effective working relationship with investigators and KOLs
• Unique knowledge for successful clinical program development and execution
• Proven ability to work both independently and in a cross functional team setting.
• Well-developed planning and resource allocation skills.
• Strong communication and presentation skills.
• Customer orientation.