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Created by jianglicat - 讲礼猫
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职位搜索/阿斯利康/Senior Programmer I/II (Oncology)
Astrazeneca logo
A
阿斯利康 (Astrazeneca)

职位信息

上海市
高级经验
全职员工
仅现场办公
本科
普通员工/个人贡献者

标签

SAS监管要求临床研究制药行业统计编程SDTMADaMCDISC
💡

核心评价

跨国药企肿瘤领域核心技术岗,社会价值感突出,技能要求专精,发展路径清晰。

Senior Programmer I/II (Oncology)

🤖 AI 估测:¥35K-55K

发布时间:25 天前

立即应聘

ℹ️关于这个职位

这是一个在跨国制药巨头阿斯利康的肿瘤领域高级统计程序员职位
你将主要负责临床研究数据的编程、验证和质量审查,确保数据符合行业标准(如CDISC)和监管要求,并支持新药研发和申报
这是一个需要深厚SAS编程技能、对制药行业有深刻理解,并能独立领导项目的技术核心岗位

✓工作职责

Key Tasks Collaboration with AZ Global Product Programmer and other R&D 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 process for 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 staffs

⭐最低要求

JOB REQUIREMENTS: Academic / Professional Qualification / Working Experience Advanced SAS programming knowledge 2 or 5+ years of working experience in Pharmaceutical industry BSc or higher degree in Mathematical, Statistical, Computer Science or Life Science or equivalent experience Technical / Skills Training 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 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

👍优先资格

Other programming languages are preferred e.g. R, S-PLUS, Python, XML etc
Watch Jobs

我们专注于实时追踪各企业最新职位动态,帮助您节省求职时间,快速找到理想工作机会。

探索

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  • 数据统计
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  • 数据方法论
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微信公众号小红书淘宝店铺

© 2026 Watch Jobs. 保留所有权利

Created by jianglicat - 讲礼猫

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