CRC临床协调员-武汉

岗位职责：
1、 派遣到临床研究机构从事临床研究的相关工作。
2、 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。
3、 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、文件归档和管理工作。
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，大专以上学历。
2、一年以上临床或CRC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. Assign to clinical trial project and work at clinical research center；
2. Assist the clinician with the non-scientific judgments of 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, document archiving and management of study materials;
4. Input clinical data into clinical trial system (English Entry).
Qualifications:
1. Junior college or above in medical science, nursing or related subjects;
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;