SMO

A Site Management Organization

We seek out medical practices that want to do clinical trials at their site, but lack the business knowledge to do so. Once engaged, we find the site studies, negotiate with pharma on their behalf, take care of regulatory, HR, financial issues. This lets the doctors at the sites focus on just the medical aspects of the clinical trial.

Facility Assessment
Contract and budget management
Coordination
Hiring and HR
Subject Recruitment and Compensation
Media Campaigns
IRB Submission
CLIA

GCP and other certifications
Compliance and Regulatory
Sponsor and FDA Audits
Site Selection
Regulatory Strategy
IRB Submission
CRF Creation
Database Setup