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Clinical Monitoring and Site Management

At Confidence Pharmaceutical Research, we recognize that continuity, trust, and transparency are critical to trial success. That’s why we partner with experienced, long-tenured Clinical Research Associates (CRAs) who remain engaged throughout the study lifecycle. In an industry where high CRA turnover is common, our low-to-zero turnover model ensures consistent communication, stronger site relationships, and better study outcomes.

How We Do It?

  • Long-standing collaborations with high-performing research sites
  • Consistent CRA-site partnerships that support protocol adherence and patient retention
  • On-the-ground insight that helps identify and resolve issues early
  • Monitoring activities guided by Clinical Monitoring Plans and Confidence SOPs
  • Compliance with ICH-GCP, regulatory authority expectations, and sponsor-specific protocols
  • Documentation of all visits via CTMS
  • Site Selection Visits (SSVs), Site Initiation Visits (SIVs), Routine Monitoring Visits (RMVs),, Close-Out Visits (COVs)
  • Remote Monitoring
  • All visits documented, traceable, and audit-ready

What Sets Us Apart?

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