Senior Programmer I/II
职位描述
RESPONSIBILITIES:*Collaboration with AZ Global Product Programmer and other TA team members to ensure alignment to corporate and TA standards and ensure implementation of functional best practice and lessons learned*In-depth critical and quality review of key study documents including but not limited to: Case Report Form, SAP and FL templates, validation plans and quality documentation, STM and analysis data set specifications, compliance to data and output standards* Plan, lead, and perform quality review or contribute to statistical programming study deliverables:SDTM and analysis (ADaM) databases, statistical reporting outputs (TFLs), including but not limited to 1.Accuracy of database structures, values and algorithms; 2, Adherence to analysis and standards requirements for study databases and TFLs 3.Accuracy and completeness of specifications and documentation* Programming and validation of deliverables to support ad ho analyses, site inspection and responses to regulatory queries etc.* Communicate technical requirements for study deliverables to biometrics vendors*Builds and maintains effective working relationships with cross-functional teams*Contribute to and critically evaluate management of operational and data risks within the cross-functional study team*Contribute to the preparation and quality review of regulatory submission packages*Identifies opportunities and contribute to the improvement of understanding and processfor quality study execution*Identifies opportunities and contributes to the development of best practice to improve quality,efficiency and effectiveness*Mentor/coach and support the education and training of junior staffsJOB REQUIREMENTS:* Advanced SAS programming knowledge* 5+ years of working experience in Pharmaceutical industry* BSc or higher degree in Mathematical, Statistical, Computer Science or Life Science or equivalent experience*Proficient knowledge of CDSIC standard and industry best practices*In-depth Knowledge of database setup and report publishing requirements*In-depth Knowledge of technical and regulatory requirements related to the role*Knowledge of statistical concept*Knowledge of the drug indications within a therapeutic area, eg. Oncology*Experience in building and maintaining effective working relationships within teams*Ability to lead project independently with strategical thinking and work on multiple tasks*Ability to prioritize and project manage to optimize support.*Excellent verbal and written communication skills*Other programming languages are preferred e.g. R, S-PLUS, Python, XML etcAstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law. AstraZeneca only employs individuals with the right to work in the country/ies where the role is advertised. 阿斯利康是一家提供平等机会的企业,我们将考虑所有符合条件的求职者就业。不因残疾、性别或性取向、怀孕或产假状况、种族或民族或族裔出身、年龄、宗教或信仰、性别认同或变更、婚姻或伴侣关系、受保护的退伍军人身份(如果适用)及任何其他受法律保护的特征而产生歧视。
企业简介
阿斯利康是全球领先制药公司,由前瑞典阿斯特拉公司和前英国捷利康公司于1999年合并而成。阿斯利康在6大治疗领域为患者提供富于创新,卓有成效的医药产品,包括消化、心血管、肿瘤、中枢神经、麻醉和呼吸等,其中许多产品居于世界领先地位。
阿斯利康总部位于英国伦敦,研发总部位于瑞典。产品销售覆盖全球100多个国家和地区。2005年公司销售收入为240亿美元。
阿斯利康拥有强大的研发能力,平均每个工作日的研发投入达到1400万美元 (2005年研发总投入为34亿美元)。我们在7个国家设有11个研发机构,共有11,900名员工从事与新药研发相关的工作。
阿斯利康拥有极具希望的早期开发产品组合,共有45个项目处于临床前研究阶段、17个项目处于一期临床研究阶段、13个项目处于二期临床研究阶段、6个项目处于三期临床研究阶段。
阿斯利康在全球19个国家有27个生产基地,共有14,000名员工致力于为客户提供安全、有效、高质量的产品。
阿斯利康在全球共有65,000名员工,从事医药产品和医疗服务的研发、生产和销售业务。
阿斯利康被列入道琼斯可持续发展指数(全球)以及显示企业良好社会责任度的富时社会责任指数(FTSE4Good Index)。
热门区域招聘: 重庆 北京 上海 浙江 江苏 广东 山东 湖南 安徽 河北
上海招聘企业: 百进冠合(海南) 医疗科技有限公司 上海华茂药业有限公司 上海信谊药厂有限公司 上海强生制药 欧姆龙健康医疗(中国)有限公司 青海瑞成药业(集团)有限公司 上海交通大学医学院附属瑞金医院 复旦大学附属中山医院 上海复星医药 上海医药集团
职位发布日期: 2023-05-18