Clinical Management

Trial Runners provides complete Clinical Management services that can be provided for all clinical trials. Our services include:

  • Execution of proper site selection, patient recruitment strategy development, focused data management and commercially relevant analysis and contingency plans
  • Negotiate clinical trial agreements and administer investigator payments
  • Investigator meeting management
  • Other tasks include development of slide presentations, meeting materials and assist with registration/travel coordination
  • Protocol development – including facilitating review process with all key contributors
  • Specialized site management with an emphasis on reinforcing key product messages and managing commercially sensitive investigator relationships
  • Commercially sensitive project management:
  • Partnership-based approach with close contact with key sponsor study team personnel
  • Study  and ad hoc update reports
  • Create and maintain study documents
  • Participate in internal team meetings
  • Team-based approach to management from the project managers, CRAs and monitors
  • All project managers attend regular leadership and management seminars/conferences
  • Clinical monitoring for all types of visits worldwide
  • Work directly with sponsor data management team for chosen outsourced company
  • Excellence in Quality Assurance
  • SOP training and adherence
  • Ongoing GCP/ICH training
  • Committed to routine internal QA audits

    • “Thank you for doing an outstanding job monitoring for us. I really appreciated it. You guys are an amazing find and I am grateful for all the work you put in. You did a really, really great job." Robert B. Huizinga Senior Director, Clinical Affairs, Isotechnika Pharma Inc.