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Dedicated Oncology Experience Delivers Pertinent, High-Quality Data in Less Time

Scimega works exclusively with full-time, permanent, local Clinical Research Associates who choose to work with us because of our singular focus on the conduct of Oncology Clinical Trials. Most have prior experience working for one or more of the over 50 Canadian cancer research centers located across the country. Together this team of oncology experts share your passion for the advancement of cutting-edge cancer research.

The rapid collection of clean and pertinent data is your key to making well-informed drug development decisions. We provide investigative teams with clear guidance and advice to simplify the study management process leading to fewer study deviations and overall visits. This is supported by our consistent CRA site assignment strategy that supports the creation of a living archive for your study activity in Canada over the long-term.

We provide peace of mind that your Phase 1, 2 & Phase 3 oncology clinical trial will be run safely, smoothly and efficiently from site selection to study close-out.

Top 3 Reasons Why Canadian Site Personnel Consider Scimega Oncology Trial Monitoring and Site Support Superior to Other CROs

  • Scimega CRAs and CTLs are actually experienced in onsite oncology trial management;
  • Scimega always deals with any questions quickly and efficiently;
  • Rather than a constant stream of demands, Scimega sends personalized, timely reminders for queries and deadlines.

The above is derived from direct, written feedback from Canadian oncology Site Coordinators.


See how Scimega’s Clinical Monitoring Services could help you manage all aspects of study operations and site level requirements.

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