Clinical Trial Management / Project Management

Our Capabilities

Depending on your requirements, from bringing in novel cannabinoid-related compounds or conducting late-phase clinical studies, we will be able to provide a turn-key solution for your needs.

Clinical Trial Management / Project Management

MCRC provides each clinical research trial with a dedicated Clinical Trial Manager to ensure that milestones are reached and timelines are met. Our clients receive effective communication and ongoing status updates throughout the process.

From the initial contact to the delivery of the final clinical trial report, our clients are kept fully informed.

Our Clinical Trial Managers are involved in all aspects of clinical trial management, including:

  • Feasibility
  • Trial design
  • Protocol review
  • Development of Patient information and consent forms
  • Review of eCRF design and development
  • Ethics Committee submissions
  • Contract Negotiation with trial sites
  • Vendor Management
  • Investigator and Site Selection
  • Review of trial monitoring reports