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; 职位福利：餐补、交通补助、弹性工作、超长带薪年假、通讯补助、定期体检、周末双休、六险一金