上海招聘

Responsibilities:

The Position

To manage, develop and enable members of CDM to maximally contribute and perform toward assigned studies, programs and initiatives. To contribute to the global CDM strategy, and ensure local implementation.

Primary Responsibilities

Coaches, supports, manages and leads staff in setting personal goals, clarifying expectations and job accountabilities.

Manages staff performance by providing feedback, evaluation and recognition on an ongoing basis.

Recruits and hires high potential staff in partnership with Human Resources.

Manages the overall contribution of individual team members to ensure the effective execution and delivery of tasks.

Ensures the PD, Biometrics and CDM mission, vision, values and goals are understood and that individuals are clear on how they contribute to them.

Ensures staff adherence to SOPs, supporting documents and processes.

Ensures staff are trained for their job and developed to maximize their contribution.

Supports staff in the creation of Development Plans and identification of opportunities.

Promotes CDM operational excellence by facilitating knowledge sharing and creating an environment of continuous improvement.

Manages local resources within global resourcing database, and components of local CDM budget.

Requirements:

BA/BS degree or equivalent

Personnel management skills or team leadership experience preferred

Proven experience in the pharmaceutical/biotech industry with an emphasis in CDM/Biometrics

Ability to communicate effectively at all levels of the organization and across cultures

Ability to build an effective, collaborative team environment

Strong project management, problem-solving and planning skills

Thorough understanding of ICH and corporate GCP regulations and SOPs

Comprehensive understanding of the conceptual basis for CDM conventions, standards and processes

Comprehensive understanding of CDM’s role in drug development

More Information related to This Position

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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。