Contact Roger Sharpe
to discuss your research project at
416.435.1746 or rsharpe@cmxres.com.

Continuous Leading Edge Proficiency


Every step is integral to the process. To stay in front you have to be the first to move: fully prepared, with dedicated effort and attention to detail.

Clinical Research Management Team: cmx is able to provide study design, protocol writing, project management, regulatory submissions, site monitoring, data management, medical monitoring, statistical analysis, final report writing and presentation/manuscript preparation.

Site Management Organization (SMO) provides you with experienced research sites and Principal Investigators in a wide range of therapeutic areas, who have distinguished themselves as integral partners in clinical development programs.

cmx manages a physician network representing over 100 physicians and 120 coordinators across Canada, including the largest Urology Network in North America. Our highly experienced clinical team of investigators and research coordinators covers a range of specialties.

The Clinical Research Coordinator Service provides temporary staffing to sites. We supply fully trained and certified CRC’s to manage work overflow at research practices. Our CRC’s ensure that research data is of the highest integrity while maximizing the project workflow.

Our Patient Recruitment Group enhances enrolment of motivated and eligible subjects for your clinical study. The cmx call centre pre-screens and refers only qualified patients, meeting research demographic and subject requirements quickly and efficiently. Our centralized advertising service gives you cost effective exposure and the highest return for your budget.

The Clinical Trial Consulting Team provides assessment of project feasibility, drug-life cycle management, market positioning and investor relations.

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