上海招聘

Responsibility:
1. Reviews and provides feedback to Scope of Work for outsourced studies with respect to the DDE subfunction's areas of responsibilities
2. Is responsible for complex deliverables for the subfunction for one or more studies
3. Contributes or leads local and subfunctional working groups and initiatives
4. Contributes to cross-functional or global initiatives
5. Leads or participates in the local functional/ cross-functional implementation of best practices and process improvement initiatives
6. Effectively communicates ideas, project goals and status of work and independently presents at department meetings
7. Identifies and develops solutions to complex problems
8. Sets targeted timeframes for deliverables and anticipates potential scenarios that may create timeline delays;
9. Able to influence and negotiate a positive outcome
10. Evaluates probability, impact and priorities of risks and develops and implements mitigation plan

Requirements

1. BA/BS degree or equivalent and moderate industry-related experience
2. Extensive practical and theoretical expertise within his or her subfunction
In-depth understanding of the business of his or her subfunction and the greater CDM organization

Experience and/or competencies required in previous job levels are met and demonstrates:

1. Significant working experience with a programming language like SQL, PL/SQL, C# or SAS and/ or significant experience in one or more areas in Clinical Data Management clinical study database setup, edit check programming, data extraction or reporting
2. Advanced understanding of the study team's role and processes in drug development
3. Advanced knowledge of clinical data management systems and processes
4. Ability to work under minimal guidance
5. Strong planning and organizational skills and the ability to manage multiple priorities, tasks or goals, developing and committing to realistic estimates and plans to complete required tasks
6. Ability to be flexible in approach to resolve issues and move forward
7. Contribution to the awareness and education of fellow subfunctional colleagues by sharing information and learnings from attendance at conferences and educational enrichment activities
8. Ability to represent at industry user groups and conferences leveraging networking opportunities
9. Articulation of functional knowledge in the development of subfunctional processes, training and related documents
10. Technical proficiency and the ability to complete complex assignments within defined parameters
11. Ability to partner with PTM Training community to ensure best training practices are being leveraged in focused training

罗氏药品临床研发亚太中心

罗氏药品临床研发亚太中心位于上海张江高科技园区，是罗氏在中国乃至亚太地区（不包括日本在内）第一个全功能临床药品开发中心，是罗氏药品开发部在全球的第五个研发地区。其前身为2007年10月成立的罗氏药品开发中国中心。

罗氏于2007年在中国率先设立全球药品开发中心，成为在华完成且体现药物研究、药品开发、生产制造和市场销售环节等整体价值链布局的跨国制药企业。此举不仅将加快新药在华的上市时间，使国内广大患者有望更早地受益于创新药物，而且将让更多的中国研究机构、学者、临床医生更早、更主动地参与到全球创新药物的开发过程。

罗氏药品开发中国中心从事药品开发工作，是把经过实验室筛选的分子转变成药物的关键一环，它通过国际多中心临床研究，鉴定药物的安全性和有效性，是驱动药物价值链的引擎。罗氏药品开发中国中心于2009年9月升级为罗氏药品临床研发亚太中心，负责罗氏在亚太地区的药品开发，令更多中国乃至亚太地区的患者尽早受益。