Job Description
When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
(a) Key working relationships / 主 要 工 作 关 系
- Internal contacts within AZ / 内 部 联 系
• Clinical Research Team
• Quality Assurance / Quality Control
• Local drug supply chain
• R&D, GMA, Global ESRO, etc
• Procurement
• Regulatory Affairs
- External contacts with organizations outside AZ / 外 界 联 系
• Principal Investigator/Co-Investigators
• CRO/SMO
• Any other vendors if related to function scope and responsibility
(b) Job requirements /工 作 要 求
• Results Driven Behavior
• Self-motivation and adaptability
• History of successful managerial experience on project management
• Ability to form strong alliances with marketing teams and among own team members
(c) Academic / Professional qualification / 学 历 / 专 业 资 格
Bachelor or higher degree in Science, Medical or Pharmaceutical Background
(d) Technical / skill training / 技 术 / 技 能 训 练
• Data Management Experience
• Knowledge of GCP, AZ SOPs and drug development and regulations
• Comprehensive knowledge of CDASH/SDTM/ADaM CDISC standards and metadata management
Skills for CRF/eCRF design
• Cross-function experience in drug development, particularly CRF/eCRF design and DM
• Ability to see cross-project dependencies and act to resolve issues
• Good presentation and communication skills across different business areas ( Internal , External)
• Effective meeting and time management
• Negotiation skills
(e) Working experience (No. of years / 年 资, Job function / 工 作 功 能, Business types / 业 务 种 类 )
I) Essential 必 需
• At least 5 relevant working experience in drug development or medical affair in a pharmaceutical company or CRO setting.
• Disease Area expertise in one or more therapy areas
II) Desirable 理 想
• Knowledge of observational studies and/or real world data
- III) Language ability / 语 言 能 力
• Excellent written and verbal communication skills in English and Chinese
- IV) Computer literacy / 电 脑 知 识
• PC/Windows application
- V) Others / 其 他