Clinical Operations Support

Strong Clinical Operations support is essential for efficient and compliant clinical trials. ACRO’s experienced staff can effectively manage and monitor all aspects of clinical trials including protocol development, site selection and qualification, study preparation activities, site training, ongoing monitoring, and close-out activities. Our Clinical Operations staff works closely as an integrated team with Data Managers, Sponsor leadership, and site staff to ensure compliance and safety throughout the project.
  • Clinical Trial Monitoring
  • Protocol Writing
  • SOP Writing
  • SSP Writing
  • Site Assessment
  • Mock FDA audits​

Site Staff Training

  • GCP
  • HSP
  • GDP
  • AE/SAE reporting
  • Data collection
  • Subject recruitment and retention
  • Investigator responsibilities
  • Presentations to Sponsors on Site Capabilities