2018
DOI: 10.14740/jocmr3602w
|View full text |Cite
|
Sign up to set email alerts
|

Present Status and Perspectives on Future Roles of Japanese Clinical Research Coordinators

Abstract: BackgroundThe 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 meet… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
7
0

Year Published

2020
2020
2023
2023

Publication Types

Select...
7

Relationship

2
5

Authors

Journals

citations
Cited by 10 publications
(7 citation statements)
references
References 20 publications
0
7
0
Order By: Relevance
“…The questionnaire asked about the investigators' characteristics such as gender, position, experience with clinical trials, ethics committee applications, interest in each study design, and desire for human and physical resources required for the smooth promotion of clinical research. Many research organizations with AROs without full functions have evolved to support industry-initiated clinical trials, but are presumably not well-equipped to promote academia-initiated clinical research by their investigators (10,11). Since this feature is considered to be common to research organizations without AROs with full functions, the desires and interests considered necessary to promote research in these organizations were determined for various occupations (physician, pharmacist, nurse, and nutritionist) and departments.…”
Section: Questionnaire Distribution and Interests Identified Through The Surveymentioning
confidence: 99%
“…The questionnaire asked about the investigators' characteristics such as gender, position, experience with clinical trials, ethics committee applications, interest in each study design, and desire for human and physical resources required for the smooth promotion of clinical research. Many research organizations with AROs without full functions have evolved to support industry-initiated clinical trials, but are presumably not well-equipped to promote academia-initiated clinical research by their investigators (10,11). Since this feature is considered to be common to research organizations without AROs with full functions, the desires and interests considered necessary to promote research in these organizations were determined for various occupations (physician, pharmacist, nurse, and nutritionist) and departments.…”
Section: Questionnaire Distribution and Interests Identified Through The Surveymentioning
confidence: 99%
“…Clinical research coordinators (CRCs), such as research nurses, are core research professionals who coordinate and manage clinical trials. 7 , 8 In South Korea, new CRCs receive 40 ​h of training, and experienced CRCs receive 24 ​h of advanced training. 7 CRCs perform tasks, such as screening study subjects, patient education and acquisition of informed consent, scheduling clinical visits and contacting study subjects, completing case report forms, observing adverse events, and liaising with researchers and sponsors.…”
Section: Introductionmentioning
confidence: 99%
“…The fabricated clinical data were used in an advertising campaign for the drug, and patients were prescribed the drug based on incorrect information. Following misconduct in clinical trials, the Japanese government established and enforced the Clinical Trials Act in 2018 [ 8 ]. It obligates clinical researchers to monitor and assure quality, observe practice criteria, and manage conflicts of interest.…”
Section: Introductionmentioning
confidence: 99%