• 招聘类型：社招
• 工作性质：全职

职位描述

Responsibilities:

1) Responsible for trial master file's establishment, collection, tracking and management in compliance with GCP/SOPs and regulatory regulations. Support Clinical Project Manager to perform document page quality/ logical check.

2) Support EC dossier preparation in study level and other study relevant documentation.

3) To provide support to project team on study supplies sourcing, procurement and distribution.

4) To provide support to Clinical Project Manager on maintaining the study status tracking and following up action log.

5) Contract management including coordinating with approval process, archiving and tracking.

6) To provide support to Clinical Project Manager on study budget calculation, gap analysis between actual cost and budget, payment processing and tracking.

7) Enhance the communication and cooperation with cross-functional teams and vendors.

8) To provide coordination on project/study meeting arrangement and logistics.

9) Mentor new CTA when applicable.

任职条件

Qualifications:

1) College degree or above, or equivalent, in medical/pharmacological/nursing/life science area is preferred. Non-medical background is accepted.

2) (1-2) years' working experience with CTA/CPA/CRC.

3) Computer literacy desirable.

4) Basic use of the English language; both written and oral.

5) Excellent oral and written communication skills.

职位要求

• 学历要求：本科及以上
• 工作经验：1年以上
• 外语要求：不需要