Clinical Trial Management

As a specialized Contract Research Organization (CRO), Pacific Clinical Research provides clinical trial management for all phases of domestic research.

Unlike larger CROs that reserve their top talent for major accounts, at Pacific Clinical Research, every client receives our A-list team. We understand that the team assigned to a project has a direct impact on its success.

Larger global CROs and smaller pharmaceutical or biotech companies often have mismatched goals and operations. Our study managers at Pacific Clinical Research bring experience from both Sponsor and CRO companies, offering expert vendor oversight and management. We ensure that your trial adheres to the highest standards, providing peace of mind for small to mid-size Sponsors.

Regulatory bodies like FDA and EMA mandate oversight of outsourced clinical trials by the Sponsor. Our experience guarantees your documentation of oversight will always be audit-ready, significantly mitigating risk for outsourced studies.

We safeguard our clients’ clinical trial investments by providing thorough and measurable oversight of global CROs. Our team has experience working with all major global CROs.

The success of a project hinges on site selection and protocol design. We bring extensive experience in assessing operational aspects of proposed studies and thoroughly vetting Investigators and site staff, even for challenging and rare patient populations.

We understand the significant investment that a clinical trial represents for our clients. Budget and timeline aren’t afterthoughts for us; instead, they are carefully monitored in a monthly accrual report, prepared in cooperation with each client to maintain transparency throughout the project lifecycle.

At Pacific Clinical Research, we’re prepared for unexpected challenges that may arise during a study. Our proven track record in recovering studies from global CROs and steering them back to success demonstrates our commitment to your project’s completion.