Patient Recruitment for Oncology Clinical Trials

Patient Recruitment for Oncology Clinical Trials

Medelis is a full service oncology clinical research company, focused on oncology clinical trials design and management, including patient recruitment, for phase I and II studies in North America and Europe.

Our team has the experience, relationships and processes for rapid patient recruitment for those hard-to-reach patient populations in complex oncology clinical trials.

We specialize in oncology, and our entire team has deep oncology trial experience and expertise — from our world-class medical advisory board to our clinical team members and medical personnel.

This critical first-hand experience in the complex issues often associated with oncology clinical trials means that highly experienced resources will be working on your study.

Full Service Oncology Clinical Research

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Medelis has handled most targets within oncology. Whether it’s a standard dose-escalation phase I trial or a complex rescue of a phase III trial, chances are that our team has handled it before.

  • 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)

Efficient Clinical Trial Planning and Execution

Our clinical team’s comprehension of the complex issues of oncology trials translates into better problem identification, decision making and superior results. We value innovation, and our experience allows us to work smarter, to maximize cost and time efficiencies on your trial.

  • A highly-skilled oncology clinical team
  • Streamlined trial planning and execution
  • Flexibility to create time and cost efficiencies
  • Fastest trial startup in the industry
  • World class oncology advisory board
  • A proactive partner you can trust

A True Partner Managing Your Trial

We’re flexible, collaborative and proactive, and able to quickly adapt to study challenges or changes in the regulatory or competitive environment. This helps to speed a drug to market, and provides the decision support to determine your next clinical move.

Tell Us About Your Study

We’d love to hear from you, and can provide feedback about your study design, investigators and patient recruitment, indications, and data collection.