Medical Monitoring

C3 Research medical monitors have both clinical and research experience to provide medical expertise and oversight for the client’s entire clinical trial process, from initial study design through final study close-out. We closely monitor the clinical integrity of the trial subjects and provide safety monitoring through the duration of the study, while working with clients as expert points of reference for investigative sites and study team members.

C3 Research offers a wide variety of Medical Monitoring services for clients’ clinical development program and overall corporate goals including:

  • Clinical development plans and protocol design input
  • Protocol development and consulting
  • Therapeutic consulting
  • Investigator brochure input
  • Provide consultation for potential safety issues or medical concerns
  • Development of specific study medical monitoring plans
  • Key opinion leader network development
  • Scientific and medical support for project management teams and sites
  • Laboratory data review
  • Medical data coding and review
  • Medical monitoring for protocol queries, site support and medical/safety issues
  • Regulatory agency support and interface
  • End of study tables and listings review and scientific manuscript drafting/review
  • Review of SAEs
  • DSMB/ DMC Member