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
Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com.
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