Roles / Responsibilities:

1. Contribute to the clinical study delivery which plays a key part in the drug development process, with many tasks involved in study start-up, execution, close-out and reporting in compliance with Good Clinical Practice and AstraZeneca processes

2. Collaborate with clinical study delivery team (Global Study Associate, Global Study Associate Manager and Global Study Leader) in taking actions to address issues as they arise.

3. Support in setting up and maintaining information in many systems of AstraZeneca, eg, Global Electronic Library, Share point, electronic Trial Master File, Study email boxes, etc.

4.  Contribute to the preparation of internal and external meetings: liaise with internal and external participants, meeting room booking, TC set up, slides compilation, binder preparation, material distribution, etc

5. Initiate, maintain and archive study documents, ensure template and version compliance

6. Document formatting and other administrative tasks, eg printing, copying, distribution etc.

7. Support China hub initiatives as appropriate

Minimum Requirement:

1. Duration of working days – full time or at least 3 working days per week for at least 6 months

2. Bachelor’s degree, in Life science/ clinical education (Medical/ Nursing/ Pharmacy)

3. Good organizational and interpersonal skills.

4. Attention to details.

5. Basic knowledge of GCP, clinical trial design, execution and operations (especially study documents) would be beneficial.

6. Computer proficiency

7. Excellent knowledge of spoken and written English

8.要保证一周至少3天，持续时间6个月及以上

实习工资是100元~150元/天，公司提供免费种类繁多的自助午餐，很好的工作环境和team氛围，入职后会有2个月的专业培训及经理带领发展。