岗位职责：

1、 派遣到知名三甲医院从事跨国药厂的国际多中心临床研究。根据GCP和研究方案要求，协助项目负责医生完成临床试验各项非科学判断工作。

2、 协助研究者进行受试者筛选、入组及随访工作。

3、 协助完成研究资料的收集、归档和管理工作。

4、 完成临床试验数据录入（英文操作系统）。

岗位要求：

1、临床医学或护理等相关专业，涉外护理优先考虑，大专以上学历

2、一年以上CRC或临床经验，有临床试验经验者优先考虑

3、英语四级以上，良好的英文读写及听说能力

4、较强的独立工作能力及团队合作精神

5、具备一定的抗压能力，并会自我心理调节。

6、工作积极主动，良好的沟通及应变能力，具备良好自我学习能力

Job Description:

1. Assist the clinician with the non-scientific judgments of international multi-center clinical trials in compliance with GCP and the protocol;

2. Assist in the screening, enrollment, and follow-up visit of subjects;

3. Assist in collecting, archiving and management of study materials;

4. Input clinical data into clinical trial system(operating system in English).

Qualificatio:

1. Junior college or above in medical science, nuing or related subjects, foreign nuing specialty will be a plus;

2. Minimum 1 year of experience as a CRC or working in clinical circumstances; clinical trial experience will be a plus;

3. CET 4 or above in English, and good command of English listening& speaking& reading & writing;

4. Ability to work independently, with a team spirit;

5. Ability in working under pressure and self-regulation;

6. Positive work attitude, good communication skill and adaptability to change, and strong self-learning ability;