Principle Medical Scientist

Job Summary

Supporting SINOVAC’s robust pipeline development, the clinical research team works closely with the R&D scientists and is dedicated to scientific design and promoting the clinical trials of drugs. As the Principle Medical Scientist, you will provide strategic perspectives on clinical decision-making regarding unmet medical needs and clinical data, further clinical development plans, and ensure efficient and compliant clinical trials. You will also bridge cooperation between SINOVAC, experts, and institutions, promote knowledge exchange, and ensure smooth R&D processes through collaboration with multiple institutions. With your team also acting as an industry insider and strategic investment think tank, you will provide forward-looking advice to ensure the scientific credibility and maneuverability of investment decisions. Your professional leadership and outstanding contributions will strive to produce results for SINOVAC’s drug R&D.

Roles and Responsibilities

1. Develop clinical drug development strategies and lead the implementation of R&D plans.
2. Responsible for reviewing and approving technical materials such as protocols, clinical study reports, and registered clinical materials for drug projects.
3. Responsible for establishing collaborative relationships with domestic and foreign research institutions and experts in relevant fields.
4. Responsible for interacting with regulatory agencies, principle investigators, technical partners, CRO, and other clinical-related institutions
5. Collaborate with the R&D department to provide medical support on product design, market positioning, and preclinical research.
6. Responsible for the research and analysis of industry medical projects, accurately analyzing industry development, providing unique insights into the latest scientific and technological advancements.
7. Assist SINOVAC in strategic investment in pharmaceutical projects. Provide judgments on medical value, clinical needs, and commercialization prospects.

Qualification and Requirements

1. Ph.D in clinical medicine, with priority given to top Chinese and international universities.
2. At least 10 years of experience in medical work for drug research and development, with preference given to candidates who have experience working in both multinational pharmaceutical and innovative biotech companies.
3. Experience in independently or jointly leading early drug development process, clinical research, and registration for market launch.
4. Familiar with experts and academic resources in at least one or more specialized disease areas, with priority given to therapeutic areas such as oncology, metabolism, and respiratory diseases.
5. Capable of independently searching for English literature, participating in international academic conferences, and engaging in academic exchange with international peers. Fluency in both written and spoken English is required.