The role and responsibility for the Project Manager is to maximize the value of clinical studies, include but not limit to well manage study timeline, quality and cost, study status delivery in a timely manner. Ensure that study implement in compliance with GxP, AZ SOPs and processes.

-Academic / Professional qualification / 学 历 / 专 业 资 格

Bachelor or higher degree in Science, Medical or Pharmaceutical Background

-Technical / skill training / 技 术 / 技 能 训 练

• Strong interpersonal skills, with the ability to work effectively with others at all levels of the organization

• Excellent process, SOP, GCP and company policy competency

• Strong presentation skills

• Proven ability to deliver training

-Working experience (No. of years / 年 资, Job function / 工 作 功 能, Business types / 业 务 种 类 )

Essential 必 需

• Minimum of 5 years’ experience in managing clinical research studies/ programs in a pharmaceutical company or CRO setting. 2-3 years of project management experience.

Desirable 理 想

• Prior experience not only as a clinical management staff, but responsible for training/ quality assurance/

• quality control/ procedural document development

• Experience in working in international and cross functional teams

-Language ability / 语 言 能 力

• Good English reading, writing, speaking & listening