Job Responsibilities:
1. Provide medical and scientific expertise in the field of prospective drug diseases, provide medical advice to the management team, and help the company implement the overall strategic objectives;
2. Develop a practical CDP for each project, and promote clinical R&D as needed to cooperate with other departments to jointly advance the project;
3. Provide professional medical/clinical support for the early detection of drugs;
4. Establish cooperative relationships with outstanding KOLs and PIs as needed, including organizing and holding regular communication meetings with KOLs and advisory boards;
5. Responsible for writing and updating the relevant parts of the Investigator's Handbook (IB);
6. Participate in the formulation and approval of the protocol outline and specific content of the implementation of the clinical trial protocol, supervise the progress of the clinical trial, and review and approve the clinical research report;
7. Formulate regulatory strategies and connect with regulatory agencies as medical experts;
8. Lead the clinical development team or CRO team, and ensure the smooth progress and seamless collaboration of clinical trials.

Qualifications:
1. Major in clinical medicine, master's degree or above, doctoral degree is preferred, 5-10 years of relevant work experience, engaged in the profession of doctor, in multinational pharmaceutical companies or large domestic pharmaceutical companies is preferred;
2. In-depth knowledge of clinical development of innovative drugs, familiar with clinical phase I, II and III trial design, hypothesis verification and data analysis;
3. Led the clinical development of innovative tumor drugs, experience in clinical development of ADC drugs is preferred;
4. Be able to earn the respect of KOLs and collect comprehensive information to support decision-making;
5. Strong communication and coordination skills and team management skills, and strong ability to work under pressure.