北京招聘

Major Responsibilities:
1. Work with study statistician and project lead to develop or review annotated CRF and programming specifications.
2. Develop SAS programs for the creation of SDTM and ADaM data sets, Tables, Listings and Figures following the standard with high quality and within milestones.
3. Perform programming activities to support other departments.
4. Provide inputs for key study documents; CRF, Data transfer specification, SAP and TFL template, etc.
5. Prepare data visualizations for Cross functional teams.
6. Provide input on process improvement initiatives and participate in non-clinical project activities.
7. Additional responsibilities as defined by supervisor/manager.
Requirements:
1. Education: Bachelor or Master degree in Biostatistics, Statistics, Computer Science or a related discipline.
2. Work Experience: 3+ years of hands-on experience in a programming role supporting clinical trials.
3. Knowledge of CDSIC standard .
4. Knowledge of SAS.
5. Good understanding of clinical trial practices and procedures.
6. Good understanding of regulatory requirements relevant to statistical programming.
7. Knowledge of Drug indications within a therapeutic area, eg. Oncology
8. Strong communication skills and influence skills.
9. Ability to work within team and work effectively in a changing environment.
10.Critical thinking and problem solving.
Other Requirements：
Location of Role: Shanghai/Nanjing
Preference: Oncology experiences preferred; Other programming languages are preferred e.g. R, Python, etc.
Language Requirements: Competent in written and oral English in addition to local language
Travel Requirements: None

传奇生物（NASDAQ: LEGN）是一家处于临床阶段的全球生物制药公司，专注于肿瘤和其他领域的新型细胞疗法的开发。目前，公司在中国、美国、欧洲拥有800多名员工。运用创新的技术手段、全球研发模式、生产策略和专业知识，公司具备强大的潜力为患者开发和制造一流的细胞疗法。传奇生物通过战略合作开发和商业化旗下主导产品西达基奥仑赛（cilta-cel），这是一种靶向BCMA的CAR-T细胞疗法用于治疗多发性***瘤患者，该药物目前正处于注册临床试验阶段。