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CRIGH - P2 - Roles identification

WHY THIS SURVEY ?
Based on the mapping of the Harmonized Core Competency Framework produced by the Joint Task Force for Clinical Trials Competency (co-lead by the MRCT Center), the Competencies for Australian Academic Clinical Trialists developed by the NHMRC and the TDR Global Competency Framework for Clinical Research developed by The Special Programme for Research and Training in Tropical Diseases (TDR) and researchers from The Global Health Network, it appears that the range of roles covered by each document is quite different. The framework of the Global Core Competencies being a direct result of the selected roles, it is most important that they reflect the activities of the end-users we are targetting. As CRIGH's reference terms for Project 2 concentrate on the professionnals involved in the design, conduct and report of non-commercial clinical trials, it appears as a good starting point to take the most comprehensive description (the TDR document in this instance) and see if we can complete or narrow things down. Thank you for taking a few minutes to answer this online survey which has been designed for that matter.
CONTRIBUTOR'S INFORMATION
ROLES
To be keptTo me modifiedTo be discarded
Data staff
Laboratory scientist
Trial pharmacist
Community engagement staff
Research nurse
Study physician
(Principal) investigator
Trial manager or Project coordinator
Quality Control monitor
ECs & IRBs
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