清远招聘

职位描述：
KEY ACCOUNTABILITIES
Responsible for executing end to end clinical data management (CDM) activities pertaining to clinical trials, including but not limited to: Oversee the process and quality of data management work contracted to a CRO, perform data integrity review. Develop data management tool and system, perform data management activities, in compliance with Hutchison Standard Operating Procedures (SOPs) and ICH-GCP guidelines.

The Clinical Data Scientist is accountable to:
？ Provides early strategic input into protocol design, contracting process focused on data management issues;
？ Oversee the process and quality of data management work contracted out to a CRO or research collaborator. Be responsible for the oversight of all data review and cleaning activities involving close interaction with project clinical research professionals
？ Proactively communicates with project team to share project status, risk assessment and outstanding item resolution status. Ensures compliance to standard key performance indicators according to process
？ Leads the development of eCRFs, database and all the other DM activities for the study handled internally by interacting with other functional area representatives;
？ Ensure the TMF maintenance of Data Management is on time with good quality.
？ Continually evaluates data management processes and applications for improvements. Lead the development and implementation of new applications and procedures. Maintains knowledge of current regulations and technologies related to the data management function.

Complexity:
？ Anticipates problems, issues, and delays, and proactively works to minimize the impact.
？ Understanding of the conceptual basis for data management conventions, standards and processes.
Ability to develop solutions to complex problems.
？ Uses rigorous, objective logic and methods to solve difficult problems with effective solutions.
？ Ability to negotiate and strategically influence stakeholders

Specialised Knowledge:
？ Clinical Data Management System experience (e.g., Clintrial, Oracle Clinical, Inform, RAVE) and understanding of database/programming concepts. Expert in the use of Data Management applications and database/file structures
？ Knowledge of the clinical development process. Good understanding of the role of data management, biostatistics and statistical programming in the drug development process.
？ Ability to apply advanced principles, theories and concepts for CDM as a whole.
？ Knowledge of industry standards and practices, e.g. CDISC.

Minimum Requirements:
？ Educated to at least Bachelor level in Medicine, Pharmacy, Biological Sciences, or health care related disciplines.
？ At least 3-year data management experience in a multinational pharmaceutical company or Clinical Research Organization (CRO)
？ Fluent oral and written English skills
？ Self-motivated, excellent in work planning and time management

Preferred Requirements:
？ Knowledge of relevant aspects of therapeutic areas, especially knowledge of oncology and immunology
？ Able to work under pressure and in a changing environment with flexibility
？ Good communication skills with the ability to communicate with both the technical and business areas.

和黄中国医药科技有限公司（简称“ 和黄医药 ”或“ Chi-Med ”）（纳斯达克 / 伦交所：HCM）是一家创新型生物医药公司，在过去20年间致力于发现和全球开发治疗癌症和自身免疫性疾病的靶向药物和免疫疗法。目前，和黄医药共有8个抗癌类候选药物正在全球开发中，并在中国本土市场拥有广泛的商业网络。

和黄医药成立于2002年，为在纽约和伦敦两地上市的和黄中国医药科技有限公司（纳斯达克/伦交所： HCM）旗下专注于新药研发业务的子公司, 研发中心坐落在上海浦东张江高科技园区，海外临床开发及注册中心位于美国新泽西，具有完备的研发平台和GMP生产基地。管理团队成员均有在知名跨国医药和生物医药企业工作的经历，参与了多个全球新药研发；公司目前有500余位来自海内外，拥有丰富新药研发经验的科研人员，8大临床在研药物、 30多项临床试验在全球开展。

和黄医药是一家致力于创新药物研发的生物医药公司，专注于发现和开发治疗癌症和自身免疫性疾病的靶向药物和免疫疗法。 自主研发的抗肿瘤新药呋喹替尼已于2018年9月获国家药品监督管理局批准上市，并于2019年11月获纳入国家医保药品目录。公司的其他候选药物，如索凡替尼、沃利替尼等，也已进入后期开发，有望在2020及2021年上市。