北京招聘

Job Description:

1.Need to organise, manage and ensure that all clinical trials are done in strict adherence to the required standards. 

2.Will also be expected to produce high quality reports within stipulated timelines  and support the Project Manager in other aspects of the trial.

Requirements:

1.Have at least 2 years of relevant experience in clinical research in healthcare, pharmaceutical and/or CRO industry 

2.possess a Bachelor degree (major in nursing, pharmacy or other science-related background) from a recognized institution.

Positive attitude 

3.Strong sense of responsibility and commitment to excel 

4.Good team player 

5.Be able to work well in a fast-paced environment.

 CMIC Group was the first company to provide CRO (contract research organization) services in Japan. Relevant laws and rules had not been established when the group was first established. The CRO Study Group (which later became the Japan CRO Association) was formed by Mr. Kazuo Nakamura, the current CEO of CMIC Group, and others to conduct promotion and public relations activities and to negotiate with the authorities for the establishment of CROs in Japan.
 Later, when the new Good Clinical Practice (GCP) regulations came into