职责描述：
1. Manage global or regional studies and will be involved in the design, conduct, monitoring, data interpretation and reporting of individual clinical trials, ensuring that all clinical studies operate to the highest ethical and safety standards and in compliance with Good Clinical Practice (GCP) and regulatory requirements.
2. Provide expert scientific and clinical input to Clinical Development, Regulatory Affairs, Biostatistics, Data Management, and other related departments.
3. As a trial level physician and medical monitor for clinical studies, have
responsibility for protecting the integrity and conduct of clinical studies whilst also providing consultation to clinical operation colleagues on protocol design questions and answering protocol related questions from site investigators.
4. Provide strategic/tactical specialist input to clinical development programs and data interpretation and maintain up to date awareness of all important advances through scientific literature, attendance at critical meetings and relationships with Key Opinion Leaders (KOLs).
5. Establish and maintain communications with clinical investigators in field of
expertise and liaise with internal and external medical community.
任职要求：
1. M.D. degree.
2. Experience specific to oncology preferred.
3. Two or more years of industry drug development experience preferred.
4. Experience in designing, monitoring and implementing clinical trials and
interpreting trial results, including an understanding of biostatistics and safety
reporting preferred.
5. Ability to communicate effectively with internal stakeholders as well as external partners and collaborators; good presentation skills.