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Dedicated oncology experience delivers pertinent, high-quality data in less time.

Scimega’s Clinical Research Associates choose to work with us because of our singular focus on the conduct of Oncology Clinical Trials. Together we 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.

By adhering to ICH/GCP guidelines we provide peace of mind that your phase I, II and III 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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