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Research Support

In addition to leading our own studies, the Centre’s other primary function is to support clinical investigators and researchers in conducting high-quality health research. From design to execution, CHÉOS provides a broad range of support services. CHÉOS staff actively manage projects that ultimately contribute to the betterment of health systems at the local, national, and international levels.

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Please scroll down for more details and to select your service from the options below.

Resources for Trainees

When embarking on a clinical research endeavour, it is imperative that you have current training to support your work. Here you will find links to pertinent modules and resources that are useful when conducting clinical research projects.

Project Management

Our seasoned research coordinators and project managers can provide study management, monitoring, and recruitment services to ensure the seamless operation of your clinical trial.

Grant Facilitation

We offer a number of services in this area, including budget and methodological consults to help you with preparing your grant submissions.

Data Management

Our dedicated team of data management experts provide a diverse range of data services, including case report form generation, database management, randomization and drug management systems creation, and data entry.

Study Methodology & Statistics

CHÉOS methodologists and statisticians can work with you to support study design and methodological planning, randomization schemes, and data analysis (including developing and carrying out a statistical analysis plan).

Health Economics

Our team of economists bring a broad range of expertise to support health research including work in the areas of personalized medicine, health technology assessment, pharmacoeconomics, cost-effectiveness analyses, decision analysis, patient preferences, and determining the impact of lost productivity.

Regulatory Affairs

CHÉOS houses regulatory and QA/QC specialists that can assist with your research start-up and application process. Our experts can deliver guidance on your ethics application, support you with understanding and applying the various regulations from governing authorities, and work to ensure that your research process meets industry standards.

KT & Program Evaluation

We understand the importance of engaging with stakeholders at all levels to enable, promote, and disseminate evidence-based treatment, practice, and policy. Our knowledge translation and program evaluation experts will facilitate the uptake of new knowledge and help to ensure the most efficient pathways to your goals and outcomes.

Trial Monitoring and Auditing

We have certified monitoring personnel on staff who can provide monitoring and auditing services, including development of monitoring plans, monitoring sites for data quality, and GCP and protocol compliance. We can provide support in the event of a regulatory or sponsor inspection of your clinical trial.

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Health research in the heart of Vancouver