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• W2167560513 abstract "The purpose of this study was to determine the standard tasks performed by clinical research coordinators (CRCs) in oncology clinical trials.Forty-one CRCs were anonymously surveyed, using a four-page self-administered questionnaire focused on demographics, qualifications, and professional experience. The survey questions on responsibilities consisted of an ad-hoc 32-item questionnaire where respondents had to rate the frequency of involvement in the listed activities using a 3-point scale. We defined as standard a task that was rated as in all or nearly all trials by at least half of the respondents.A response rate of 90% (37 out of 41) was achieved after two mailings. Less than half of the respondents had received additional training in oncology, clinical research or Good Clinical Practices (GCP). Overall, all standard tasks performed by CRCs were in the category of monitoring activities (those usually performed by a Clinical Research Associate CRA) and included patient registration/randomization, recruitment follow-up, case report form completion, collaboration with the CRA, serious adverse events reporting, handling of investigator files, and preparing the site for and/or attending audits.CRCs play a key role in the implementation of oncology clinical trials, which goes far beyond mere data collection and/or administrative support, and directly contributes to the gathering of good quality data." @default.
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• W2167560513 date "2004-03-25" @default.
• W2167560513 modified "2023-10-18" @default.
• W2167560513 title "The role of the clinical research coordinator – data manager – in oncology clinical trials" @default.
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• W2167560513 doi "https://doi.org/10.1186/1471-2288-4-6" @default.
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