We are building upon our long-term commitment to patients by developing a whole new class of novel molecules in oncology, general medicine, inflammation and rare disease – and we need top talent to ensure these molecules become medicines and realize their potential for helping patients. **Accountabilities** + To serve as local development lead for phase I-III clinical development of Amgen Pipelines + To contribute to define, design, and execute clinical development as a strategy for drug development in China. + To serve as key role in external collaboration and strategic partnership with key local sites in clinical studies and related research area + To represent Medical Sciences internally and externally, contributing local medical insight into experimental design and data analysis. + To provide subject matter expertise in clinical and translational trial science as well as the biology and treatment. **Responsibilities:** + Lead and/or contribute to designing, gaining approval of and executing high quality development strategy for assets in China, collaborating with cross-function local colleagues and global partners, together with key functional stakeholders and governance bodies + Support the development and execution for clinical trials in China and be the local/regional medical science expert in resolving significant issues that may affect the studies + Work closely with local/regional/global cross functional colleagues, including Clinical Operations, Patient Safety and Regulatory counterparts, to provide medical expertise to the study team + Share local/regional clinical/scientific input during the development and execution of clinical trials + In defined situations working under the Global Development Lead to : + Contribute or lead development of and co-author clinical study protocol and related documents for example Key Design Elements (KDE), Clinical Study Reports (CSR), and clinical scientific publications (CSP). + Serve as a member of the CST-LT, provide medical and strategic oversight to the study execution. + Monitor, analyse, and interpret clinical study data + Contribute to the preparation of documents required for regulatory submissions + Develop and interface with local/regional industry key opinion leaders and manage scientific presentation at advisory boards, key scientific meetings and external committee meetings + Participate in interactions with regulatory agencies + Support the local/regional Brand Team in the brand planning process to ensure alignment between medical and brand activities, and help providing interpretation of clinical study data + Ensuring compliance with GCP across clinical trials **Output** + Ensure local/regional/global clinical studies are adequately and timely supported and executed + Ensure medical support leading to successfully submission and approval of CTNs and MAAs + Establish and maintain appropriate relationship with local/regional industry key opinion leaders and medical communities **Skills and Qualities** + MD degree from an accredited medical school, and experience in patient care required + Minimum 5 years of clinical research experience in academia and/or biopharmaceutical industry (biotech, pharmaceutical or CRO company) + Demonstrate in-depth knowledge in the specific therapeutic areas of oncology, general medicine, inflammation or rare disease + In-depth understanding of the scientific method and clinical applications based on medical, scientific and practical rationale + Familiarity with concepts of clinical research and clinical trial design, including working knowledge of statistics as applied to clinical trial design and analysis + Previous experience in early and/or late-stage clinical trials and regulatory filings + Ability to effectively present ideas and document complex medical/clinical concepts in both written and oral communication + Experience in writing and editing scientific research reports + Thorough understanding of GCP and familiarity with relevant NMPA and ICH guidance + Ability to collaborate effectively in and/or lead cross-functional teams + Strong commitment to goals and timelines + Ability to absorb new information quickly and gain command of relevant literature + Possessing excellent problem-solving & decision-making skills + Excellent written and verbal communication skills, including fluency in English