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首页> 外文期刊>Journal of Clinical Medicine Research >Present Status and Perspectives on Future Roles of Japanese Clinical Research Coordinators
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Present Status and Perspectives on Future Roles of Japanese Clinical Research Coordinators

机译:日本临床研究协调员的现状和未来角色的展望

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Background: The new Clinical Trials Act that recently came into effect in Japan emphasizes the reliability of investigator-initiated clinical trials. Although Japanese clinical research coordinators have been mainly engaged in operational roles in industry-initiated clinical trials for drug approval (registration trials), broadening their contribution to cover more types of clinical research may lead to quality improvement of clinical research. To ultimately establish a clinical research infrastructure that meets the needs of the new era of Clinical Trials Act, here we gathered basic information on how clinical research coordinators might make such contributions. Methods: We conducted a survey using self-reporting questionnaires in clinical research-related personnel to examine present status and the perspectives toward broader contribution of clinical research coordinators. The study participants were attendee of group discussion of a clinical research-related meeting in Shikoku area of Japan held in August 2017. Results: Among 88 participants, 69 responded (response rate: 78.4%) and 68 respondents (98.6%) were engaged in support and management of clinical research. The main area of involvement was industry-initiated registration trials (48, 69.7%), and main roles of involvement were cooperators who plays roles under the guidance of investigators (41, 59.5%). When divided by occupation into clinical research coordinators (n = 41) and other clinical research-related personnel (n = 28), approximately half of the respondents in each group replied positively to wanting broader involvement of clinical research coordinators as a clinical research professional. Conclusion: The present study revealed that about half of the clinical research coordinators and other clinical research-related personnel view a broadening of involvement of clinical research coordinators in research activities positively. Accordingly, a structured practical program aimed at encouraging such involvement may help to expand and strengthen their contribution into the future. Whether greater involvement of clinical research coordinators in clinical research will help to ensure the reliability of investigator-initiated clinical research warrants further study.
机译:背景:最近在日本生效的新《临床试验法》强调了研究者发起的临床试验的可靠性。尽管日本临床研究协调员主要在行业启动的药物批准临床试验(注册试验)中担任运营角色,但扩大其贡献范围以涵盖更多类型的临床研究可能会改善临床研究的质量。为了最终建立满足新时代《临床试验法》要求的临床研究基础设施,我们在这里收集了有关临床研究协调员如何做出此类贡献的基本信息。方法:我们对临床研究相关人员进行了自我报告调查,以调查其现状和对临床研究协调员的广泛贡献的观点。研究参与者参加了于2017年8月在日本四国地区举行的临床研究相关会议的小组讨论。结果:在88名参与者中,有69名受访者(回应率:78.4%)和68名受访者(98.6%)参与其中。临床研究的支持和管理。参与的主要领域是行业启动的注册试验(48,69.7%),参与的主要角色是合作者,他们在研究人员的指导下发挥作用(41,59.5%)。按职业划分为临床研究协调员(n = 41)和其他与临床研究相关的人员(n = 28)时,每组中约有一半的受访者表示积极地希望将临床研究协调员作为临床研究专业人员进行更广泛的参与。结论:本研究表明,大约一半的临床研究协调员和其他临床研究相关人员对临床研究协调员广泛参与积极的研究活动持积极态度。因此,旨在鼓励这种参与的结构化实用方案可能有助于扩大和加强其对未来的贡献。临床研究协调员更多地参与临床研究是否有助于确保研究者发起的临床研究的可靠性值得进一步研究。

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