職位描述
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機(jī)會(huì)的企業(yè)，我們將考慮所有符合條件的求職者就業(yè)。不因殘疾、性別或性取向、懷孕或產(chǎn)假狀況、種族或民族或族裔出身、年齡、宗教或信仰、性別認(rèn)同或變更、婚姻或伴侶關(guān)系、受保護(hù)的退伍軍人身份（如果適用）及任何其他受法律保護(hù)的特征而產(chǎn)生歧視。
