CRA I/II/Senior, 临床监查员没经验可以吗(CRA I/II/Senior, 临床监查员月薪有多少)

CRA I/II/Senior, 临床监查员没经验可以吗(CRA I/II/Senior, 临床监查...)
CRA（Clinical Research Associate）I/II/Senior是指不同级别的临床研究监查员，负责监督临床试验的执行，确保试验的合规性和数据的准确性。没有经验的应聘者如果具备医学、药学或相关领域的学历背景，以及良好的沟通能力和学习能力，可以通过公司培训和实践逐步适应这一职位。CRA的主要职责包括制定监查计划，与研究团队沟通，收集和审核临床数据，以及处理临床试验中的问题。发展前景方面，CRA可以根据个人业绩和能力晋升为高级临床监查员、临床项目经理或更高级的科研管理职位。

学历要求：本科
工作经验：2年及以上
公司性质：外资（欧美）
公司规模：10000人以上  Basic Function：
1.To perform clinical monitoring activities of designated projects in accordance with the Parexel's SOPs (or the Sponsor’s SOPs as appropriate), which include: investigator/site selection, managing and coordinating site related activities, collating regulatory documentation and IRB submissions, and monitoring activities (such as source data verification, drug accountability, etc.) throughout the study in accordance with the ICH GCP guidelines.
2.Also accountable for detecting, analyzing and solving technical, procedural and/or motivational problems that may occur to the site staff of the investigation team and thus affect the progress of the project.
3.Supporting local issues like SSU, project local issues; monitoring within the region. Requirement and Qualification:
1.A bachelor (or above) degree in a life science (preferably paramedical) field.
2.More than 2 years’ work experience in clinical operations, particularly study monitoring.
3.Good communication skill and proactive attitude.
4.Ability to take initiative and work independently.
5.Ability to speak and read the language(s) used locally in the country, plus a fluency in written and spoken English.
6.Ability to travel – on both local and international trips.