1）Responsible for formulating product medical plans and strategies based on company products, national pharmaceutical industry policies and industry development trends;
2）Lead (or direct the subordinate to carry out) the development, implementation and full management of post-launch medical research projects, including (but not limited to) expert communication, program discussion revision, guidance and supervision of CRA or MSL and data analysis & summary publication, follow-up medical clinical research progress ；
3）Responsible for product life cycle management, and provide evidence for products at different stages of development by promoting research ；
4）Build and maintain a KOL network and establish a company expert database;
5）Track medical information in relevant fields, and independently or instruct subordinates to carry out product medical knowledge base update and training;
1）Graduate degree or above in clinical medicine or other related majors;
2）More than 10 years of experience in medical affairs management, familiar with the fields of tumor/cardiovascular/neural;
3）Excellent team leadership and internal and external communication and coordination skills
4）Familiar with national laws and regulations on clinical trials, with independent medical research capabilities.
5）Keen market insight; strong judgment and decision-making ability.