Oncology Contract Clinical Research


As a single-source provider for clinical trial planning, trial management and drug development planning, Medelis is helping biotechnology and pharmaceutical companies by delivering the best total solution—and all the support required—to optimize the return on your clinical research investments. And we accomplish that in the quickest, most responsive way possible.

What we can do for you

Clinical Answers, Faster

Our approach is driven by a critical mass of clinical research expertise, the ability to identify and focus on the most significant challenges, and your need for prompt results.

Our world-class insight and experience in the development and execution of clinical research plans and protocols delivers the decision support you need to chart your next clinical move.

Medelis provides the following services to oncology sponsors:

  • Site identification, qualification and management
  • Investigator identification and recruitment
  • Patient recruitment and accrual
  • Project management and monitoring
  • Medical monitoring
  • Data management and biostatistics
  • Biostatistics analysis and reporting
  • Quality assurance and regulatory compliance
  • Medical writing
  • Protocol development (leveraging our Medical Advisory Board)

In addition to our permanent operations in North America and Europe, we use a partnership model that enables us to execute trials as needed in almost any country.

This flexibility allows us to access the best sites and patient populations for specific trials while eliminating costly overhead and the need to maintain a network of offices around the globe.