Study Management and Monitoring

We assist you in managing your study effectively within your resources and budget

  • Clinical Study Support: For early stage investigators or established investigators with larger projects
  • Develop study Manual Of Procedures
  • Develop and maintain study regulatory binders
  • Develop study specific logs and documents
  • Develop and provide access to a collection of Standard Operating Procedures
  • Develop study protocols
  • Assist in recruitment and enrollment in clinical trials and studies
  • Clinical Research Coordinator selection, interviews, and oversight
  • Access to interpreters
  • Work with PI to establish a monitoring plan
  • Conduct study monitoring visits/checks