Onco Clinician (Contractor)-Shanghai/Beijing

辉瑞中国招聘肿瘤临床医生（合同制），负责临床试验的设计、执行与医学监督，确保高质量数据交付，并作为临床试验现场联络人，支持研究者合作与项目推进

Co-chair clinical study team and collaborate with study team members. 2. Point of accountability for design, conduct, interpretation and reporting of clinical studies. 3. Provide clinical and scientific expertise to trial strategy and protocol development. 4. Design/write clinical trial outlines, protocols and amendments. 5. Identify and assess study risks; create and implement mitigation plans. 6. Provide clinical input to monitoring guidelines, statistical analysis plans, informed consent, etc. 7. Contribute to CRO/vendor selection. 8. Approve selection of countries, sites and investigators. 9. Ensure study registration and results disclosure. 10. Create clinical/protocol training materials. 11. Establish and oversee Data Monitoring Committees and endpoint adjudication committees. 12. Jointly accountable for study enrollment and timelines. 13. Maintain direct contact with investigative sites. 14. Perform regular review of individual and cumulative safety data. 15. Identify emerging safety trends and escalate. 16. Review and manage protocol deviations. 17. Conduct clinical review and interpretation of efficacy and safety data. 18. Deliver top-line reports and clinical study reports. 19. Responsible for clinical and scientific validity of study report. 20. Ensure narrative strategy consistency. 21. Write safety narratives. 22. Assist in regulatory compliance. 23. Contribute to primary publication. 24. Act as primary contact for clinical/medical questions. 25. Keep Clinical Program Lead informed of critical issues. 26. Present to internal and external advisory committees.