The Critical Role of the Clinical Research Coordinator for Clinical Trials: A Survey in Oncology

Author:

Cinefra Margherita1,Cagnazzo Celeste2,McMahon Laura3,Arizio Francesca4,Campora Sara5,Camisa Roberta6,Canzanella Giuliana7,Contu Marianna8,Frati Paola9,Sottile Roberta10,Gori Stefania11,Procopio Giuseppe12,Nanni Oriana13,

Affiliation:

1. Medical Oncology and Breast Unit, “A. Perrino” Hospital, Brindisi - Italy

2. Fondazione del Piemonte per I'Oncologia (FPO), Candiolo Cancer Institute (IRCCS), Candiolo (TO) - Italy

3. Istituto Oncologico Veneto IRCCS Padova, Padova - Italy

4. Department of Oncology, University of Turin, AOU San Luigi, Orbassano, Italy

5. SC Oncologia Medica, E.O. Ospedali Galliera, Genova - Italy

6. UOC di Oncologia Medica, Azienda Ospedaliero-Universitaria di Parma, Parma - Italy

7. Unità Sperimentazioni Cliniche, Istituto Nazionale Tumori – IRCCS – Fondazione G. Pascale, Napoli - Italy

8. UOC di Oncologia Medica, Azienda Ospedaliero-Universitaria di Sassari, Sassari - Italy

9. Unit of Immunotherapy of Human Tumors, Fondazione IRCCS, Istituto Nazionale dei Tumori, Milano - Italy

10. Department of Oncology, Azienda Sanitaria Universitaria Integrata di Udine, Udine - Italy

11. Oncologia Medica, Ospedale Don Calabria - Sacro Cuore, Verona - Italy

12. Divisione di Oncologia Medica 1, Fondazione IRCCS, Istituto Nazionale dei Tumori, Milano - Italy

13. Biostatistics and Clinical trial Unit - Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) Srl IRCCS Meldola (FC) - Italy

Abstract

Introduction Access to innovative medicine requires proper evidence from clinical trials with the growing demand of qualified and experienced personnel. The clinical research coordinator (CRC) plays an important role in the conduction of research activities and provides a strong support to the research team. In Italy, this role is not recognized at any institutional level and its professional outline is still indefinite. Several national associations (Associazione Italiana di Oncologia Medica, Collegio Italiano dei Primari Oncologi Medici Ospedalieri, Gruppo Italiano Data Manager) are committed to promoting the enhancement and recognition of the professional status of CRCs, underlining their role as fundamental. Methods A web survey, proposed by the AIOM CRC Working Group, was submitted to 319 Italian oncology sites with items focusing on the organization of sites, the research activities, the staff composition, and the presence of coordinators and the multidisciplinary team. Results A total of 115 sites (35.9%) responded to the web survey. Clinical studies were carried out at 88.7% of the investigated sites, and coordinators were on staff at 75.5% of the active investigational sites. Interestingly, there was a direct association between the number of clinical studies and the number of coordinators, whose contribution to the research activities is believed to be essential for trial conduct in 82.4% of cases. Most sites retain that the quality of clinical research has absolutely improved (83.3%) after the implementation of a coordinator as member of the team. Conclusions Given the constant growth of the number of clinical trials performed at Italian oncology sites, the CRC proves to be an essential component of the research team. However, there is an urgent need to institute the professional role alongside the need to standardize the training of coordinators to establish the minimum requirements enhanced by qualifying courses.

Publisher

SAGE Publications

Subject

Immunology

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