Clinical Services > Clinical Site Monitoring

Clinical Site Monitoring


Exceptionally trained, regionally based Clinical Research Associates (CRAs) with an average of 10+ years clinical trial industry experience and over 1000 site visits in the past three years


Key advantages to partnering with PRC Clinical for Clinical Site Monitoring:

  • PRC Clinical CRAs ensure that for every project, investigators are appropriately selected and trained to complete the study following GCP and ICH guidelines in order to produce high-quality study results.
  • Familiar with all EDC platforms
  • Our CRAs maintain a strong relationship with each study site, ensuring absolute quality and on-time receipt of all clinical trial deliverables.
  • Site focused CRAs that integrate with Sponsor teams and facilitate communication between sites and sponsors
  • Supported by ongoing trainings to remain current with industry content and trends
  • Developed and maintained full SOPs (Standard Operating Procedures)