北京招聘

-Responsible for study filing, tracking and archiving. Ensure these activities performed in compliance with GCP/SOPs and CSP.

-Responsible for study administrative supports in compliance with company policy.

-Develop and maintain excellent working relationships with external and internal customers to ensure the smooth and timely delivery of clinical studies.

-If need, Perform other tasks assigned by line manager。

-As required, assist CRAs with particular in house works.

Basic Requirements:

1.      Bachelor degree.

2.      Excellent professional, organizational and interpersonal skills.

3.      Ability to work independently, self-starter, work under pressure, accept responsibilities and learn new tasks.

4.      Good communication with study team, vendors, Team work.

5.      Good computer skills including proficiency with Microsoft Word, Excel, Explorer and Outlook.

6.      At least two-year administrator experience in Global industry or CRO.

  

Our mission is to build a preeminent biopharmaceutical organization to develop and commercialize globally innovative products in Greater China and other emerging Asia Pacific markets.

Our advantage includes an insight-driven, highly productive business development engine and world-class clinical and regulatory teams, supported by a substantial financial foundation.