Clinical Trials Consortium.

CTC Background


At the 2017 MICYRN Strategic Retreat and following the merging of MICYRN and CCCHR (The Council for Canadian Child Health Research), there was a consensus that the organization should prioritize its activities with its primary objective being to develop a collaborative national infrastructure to support clinical investigations, with an emphasis on multi-centre clinical trials. The ultimate goal of this consortium is to enhance Canadian child health through increased access to high-quality clinical trials supported by an efficient, safe, and family-centered national infrastructure. Contributions to the national infrastructure at the local site level and broadly encouraging each site to invest in this initiative to enable the development of key deliverables will be imperative if this is to be successful at the national level.

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Mandate


The Clinical Trials Consortium (CTC) will prioritize areas of opportunity and develop scientific and operational directions and initiatives. It will engage individuals who have responsibility for overseeing clinical research operations or who are invested in developing clinical research at their member-affiliated MICYRN research organizations across the country.

Increased communication with MICYRN member research organizations will better support multisite projects and investigator teams, and help identify common processes that could benefit from being harmonized across institutions through the development of tactical approaches to realize shared efficiencies.

The CTC will also identify key areas where setting best practices could enhance the quality and outcome of research (i.e., data management, biobanking); and determine means by which to enact best practices. In addition, it will provide input into MICYRN performance metrics and return on investment for MICYRN. Finally, the group will establish and build on opportunities to generate interest in trials from industry and forge international relationships to improve the situation for clinical trials at home and beyond.

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Consortium Members


Click here for full member bios.

Anthony Chan McMaster University
Ashton Chugh ACHRI
Brandy Wicklow CHRIM
Bernadette Druken Janeway Pediatric Research Unit
Bruno Piedboeuf Université Laval
Darryl Adamko University of Saskatchewan
Dory Sample WCHRI
Entela Zaffino SickKids
Evdokia Anagnostou Bloorview Research Institute
Frederic Dallaire Université de Sherbrooke
Geneviève Legault Université de Sherbrooke
Jagdeep Walia Queen's University
Jason Berman CHEO
Jennifer Claydon BCCHR
Jennilea Courtney CHEO
Julia Upton SickKids
Kathleen Leadon IWK Health Centre
Lauren Kelly CHRIM
Lindsay Akrong McMaster University
Lise Bourrier CHRIM
Megan Stewart Bloorview Research Institute
Michael Esser ACHRI
Michael Rieder Western University
Nathalie Bureau CHU Sainte-Justine
Nicole Chabot Université Laval
Patti Li McGill University
Paul Moorehead Janeway Pediatric Research Unit
Quynh Doan BCCHR
Sandra Davidge WCHRI
Soren Gantt CHU Sainte-Justine
Steven Beyea IWK Health Centre
Tanya Voth WCHRI
Tova Dybvig University of Saskatchewan

 Clinical Trial Consortium Documents

Please contact your organization’s representative (above) for access to archived meeting notes and administrative files.