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3-4年经验 -
本科 -
招若干人 -
11-09 发布
- 五险一金
- 补充医疗保险
- 补充公积金
- 免费班车
- 年终奖金
- 出国机会
- 通讯补贴
- 餐饮补贴
职位描述
职位描述： Leads and/or contributes to:The development of the clinical study database and all components. This in collaboration with the Study Data Manager, who provides the core specifications.The development of reports and visualizations outputs for data cleaning, clinical narratives and reconciliation activities. This in collaboration with the Study Data Manager and other customersThe development of data transformation programs, including specifications according to CDISC and Roche data tabulation standardsSelects and implements appropriate study conventions, including data collection and data tabulation standards, knowledge sharing and best practices on assigned study(s).Communication:Effectively communicates with SDM, study team, Functional Service Providers and stakeholders on Clinical Study Database, Reporting and Transformation requirements and status of workShares functional knowledge using relevant forums and communication toolsEffectively partners with SDM for representation on study team for Clinical Programming related topics and deliverablesStrategic Agility:Manages Clinical Programming deliverables, including timelines, risks and coordination of cross-functional tasks with strong understanding of downstream processes and stakeholder needs and impactsIdentifies Clinical Programming related issues appropriately and addresses corrective action plansEvaluates the impact of risks, develops and implements mitigation plans at study levelFeedback & Coaching:Provides coaching and mentoring to clinical programming colleaguesProvides timely feedback to individuals and Management, and seeks ongoing feedback for personal developmentTeamwork & Collaborations:Fosters teamwork.Develops and maintains working relationships and networks within and outside of CDM at the study level and project levelQualifications:BA/BS degree or equivalent and moderate industry-related experienceModerate practical and theoretical expertise within his or her disciplineIn-depth understanding of the business of his or her discipline and the wider CDM organization 职能类别： 临床数据分析员
联系方式
龙东大道1100号
公司信息
罗氏全球药品开发中心－上海是罗氏的全功能临床药品开发中心，关键治疗领域包括肿瘤学、免疫学、眼科、传染病学、代谢学以及神经科学。 罗氏全球药品开发中心－上海前身为2007年10月成立的罗氏药品开发中国中心，该中心于2009年9月1日升级，成为罗氏全球五大药品开发中心之一。 该中心的设立意味着罗氏制药在中国的发展进入了一个新的领域，标志着罗氏在华完成了药物研究、药品开发、生产制造和市场销售环节等整体价值链的布局。
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