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

Career Opportunities


CMX Research Inc. is continually searching for the best and brightest candidates to join its team of skilled professionals. To apply for a specific position listed below, send your cover letter and CV to info@cmxres.com or submit your updated CV that will be kept on file and matched to opportunities that may become available in the future.


Current opening:

Position Title: Clinical Research Coordinator

Position Summary:
We are currently recruiting for full and part-time Clinical Research Coordinator for our affiliated site in London, Ontario,  Toronto, Mississauga, and the surrounding GTA, and Quebec.


Responsibilities include but are not limited to:

  • Participating and overseeing study set-up,
  • Assist in consenting patients to participate in clinical trials
  • Patient screening for clinical trials,
  • Conduct/assist with the study procedures
  • Completion of source documents ,CRFs, and  of regulatory documents,
  • Data query resolution
  • Participate in office activities during study days and clinic visits
  • Participate in sponsor visits including site selection, study initiation, study monitoring and study closure
  • Provide effective communication to research “team” including preparation and delivery of protocol, and orientation to ensure an understanding of their responsibilities related to the conduct of the study
  • Communicate with sponsor to ensure study is being conducted to sponsors satisfaction and follow up on deficiencies
  • Ongoing general office and administrative duties within practice
  • Weekly reporting of enrollment and study status to CMX Research Inc.

Qualified candidates will possess the following knowledge and skills:

  • Degree in a health related discipline. A strong preference is given towards a nursing degree with coordinator certification as a “Research Coordinator”
  • Minimum of one year experience, or equivalent industry experience with site interaction is preferred
  • Knowledge of ICH/GCP, and other applicable regulatory guidelines. Understanding of clinical research and drug development processes
  • Excellent organizational, problem-solving, multi-tasking, computer, verbal and written communication skills
  • If not certified, agreement to enroll in a certification program

Send resumes to: info@cmxres.com
Please indicate desired location/city of work



 


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