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?
- Trusted Relationships with Sites and Investigators
- 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
- Structured, Transparent Monitoring
- 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
- Comprehensive Monitoring Coverage
- 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?
- Exceptionally low CRA turnover ensures site consistency from startup to close-out
- Long-standing relationships with trusted investigators and site teams
- CTMS-powered transparency for full sponsor visibility and oversight
- Flexible visit models—on-site and remote—tailored to study needs
- Monitoring aligned with global and local regulations, GCP, and sponsor requirementsList Item