Medical Manager

Responsibility

• Analyze academic developments in the field of innovative drug industry；

• Provide clinical information and opinions during project initiation and product development；

• Lead medical affairs in the process of clinical research, including but not limited to protocol, IB, CSR writing or review. Establish cooperation with CRO or other relevant teams to promote the clinical trial and marketing of products；

• In the process of clinical research project development and application, cooperate in discussing medical work such as enrollment review, AE/ADR review, medical supervision and audit, ensure CRO medical services and researchers play a corresponding role, and guide the project medical problems to be solved in favor of the sponsor and in accordance with the requirements of laws and regulations；

• Participate in the preparation, improvement and updating of relevant SOP; • Cooperate with relevant departments to organize and manage academic conferences；

• Undertake the systematic management of clinical PV of new drugs of the company, and standardize the connection between project PV and company PV.

Qualification

• Master's degree or above is required, and clinical medicine and other related majors and doctorates are preferred；

• More than three years of pharmaceutical related work experience；

• Have excellent project organization, management and coordination capabilities；

• Be familiar with the clinical trial process of drugs；

• Have good communication skills of researchers and CRO medical services.