Du Can, Han Qi, Lu Ziqian, Li Jia
National Clinical Research Center for Oral Diseases, Clinical Research Department, West China Hospital of Stomatology, Sichuan University, Chengdu, Sichuan, China.
Front Med (Lausanne). 2025 Jan 23;12:1499237. doi: 10.3389/fmed.2025.1499237. eCollection 2025.
Clinical research associates (CRAs) are the sponsor's representatives, monitor the process and quality of clinical trials, their professional quality can affect the quality of clinical trials. But there is a conflict between the large number of CRAs personnel and unsatisfactory quality of clinical trial monitoring, and the reason is unknown. Therefore, our study investigated the occupational status of CRAs through a questionnaire survey. A total of 401 eligible questionnaires were included in the final analysis. Of whom, 71.32% were females, the average age is 27.86 years (range: 22-46 years), 95.01% had a bachelor's degree or above, and 60% had a pharmaceutical major. 76.31% had month income of <20,000 Yuan RMB, and dissatisfied with their current salary level. Over 80% weekly working time more than 40 h. 79.3% CRAs traveling for less than 7 days per month under the impact of the COVID-19 epidemic. 80% of them are satisfied with promotion channels and company training. Furthermore, Through the analysis of satisfaction differences, we found that CRAs with different educational backgrounds have significant differences in career satisfaction. It was suggested by more than 80% CRAs that the application materials for clinical trials should be unified nationwide and an ethical mutual recognition system. In conclusion, our study is the first large-scale survey of CRAs in China, the current professional situation of CRAs is considerable, but overall it still needs further improvement and enhancement, the monitoring difficulties faced by CRAs mainly come from hospitals, companies, and themselves. With the robust growth of clinical trials in China, hospitals and companies need to improve the professional quality and status of CRAs through a series of measures, further driving the improvement of clinical trial quality.
临床研究协调员(CRAs)是申办方的代表,负责监测临床试验的过程和质量,他们的专业素质会影响临床试验的质量。但CRAs人员数量众多与临床试验监查质量不尽人意之间存在矛盾,原因不明。因此,我们的研究通过问卷调查对CRAs的职业状况进行了调查。最终分析纳入了401份合格问卷。其中,71.32%为女性,平均年龄为27.86岁(范围:22 - 46岁),95.01%拥有本科及以上学历,60%为药学专业。76.31%的月收入低于20,000元人民币,且对当前薪资水平不满意。超过80%的人每周工作时间超过40小时。在新冠疫情影响下,79.3%的CRAs每月出差时间少于7天。80%的人对晋升渠道和公司培训感到满意。此外,通过满意度差异分析,我们发现不同教育背景的CRAs在职业满意度上存在显著差异。超过80%的CRAs建议临床试验申请材料应在全国范围内统一,并建立伦理互认体系。总之,我们的研究是中国首次对CRAs进行的大规模调查,CRAs目前的职业状况尚可,但总体仍需进一步改进和提升,CRAs面临的监查困难主要来自医院、公司和自身。随着中国临床试验的蓬勃发展,医院和公司需要通过一系列措施提高CRAs的专业素质和地位,进一步推动临床试验质量的提升。