崗位職責(zé)：
1、 協(xié)助臨床研究機構(gòu)從事臨床研究的相關(guān)工作。
2、 根據(jù)GCP和研究方案要求，協(xié)助項目負(fù)責(zé)醫(yī)生完成臨床試驗各項非科學(xué)判斷工作。
3、 協(xié)助研究者進(jìn)行受試者篩選、入組及隨訪工作。
4、 協(xié)助完成研究資料的收集、文件歸檔和管理工作。
5、 完成臨床試驗數(shù)據(jù)錄入（英文操作系統(tǒng)）。
崗位要求：
1、臨床醫(yī)學(xué)或護(hù)理等相關(guān)專業(yè)，大專以上學(xué)歷。
2、一年以上臨床或CRC經(jīng)驗，有臨床試驗經(jīng)驗者優(yōu)先考慮。
3、英語四級以上，良好的英文讀寫及聽說能力。
4、較強的獨立工作能力及團(tuán)隊合作精神。
5、具備一定的抗壓能力，并會自我心理調(diào)節(jié)。
6、工作積極主動，良好的溝通及應(yīng)變能力，具備良好自我學(xué)習(xí)能力。
Job Description:
1. Assist 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;
3. Assist in the screening, enrollment, and follow-up visit of subjects;
4. Assist in collecting, document archiving and management of study materials;
5. 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.