该职位来源于猎聘 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

• Assign to clinical trial project and work at clinical research center；
• Assist the clinician with the non-scientific judgments of clinical trials in compliance with GCP and the protocol;
• Assist in the screening, enrollment, and follow-up visit of subjects;
• Assist in collecting, document archiving and management of study materials;
• Input clinical data into clinical trial system (English Entry).
  
  

Qualifications

• Junior college or above in medical science, nursing or related subjects;
• Minimum 1 year of experience as a CRC or working in clinical circumstances; clinical trial experience will be a plus;
• CET 4 or above in English, and good command of English listening& speaking& reading & writing;
• Ability to work independently, with a team spirit;
• Ability in working under pressure and self-regulation;
• Positive work attitude, good communication skill and adaptability to change, and strong self-learning ability;