Clinical Operations
Study Management
Site/Investigator Identification and Qualification
Central IRB Submissions
Study Monitoring
(including risk-based with biostatistics services)
Site Management
Investigational Product Management
Trial Master File Management
Study Specific Plan Development
ICF Development
Source Document Development
Vendor Management
Study Quality Risk Identification
and Management
Study Management
Site/Investigator Identification and Qualification
Central IRB Submissions
Study Monitoring
(including risk-based with biostatistics services)
Site Management
Investigational Product Management
Trial Master File Management
Study Specific Plan Development
ICF Development
Source Document Development
Vendor Management
Study Quality Risk Identification
and Management
Clinical Operations Services
With decades of experience on both the sponsor and CRO sides of drug development, our clinical operations team functions proactively by anticipating and preparing solutions for potential challenges. Our approach ensures trials progress in adherence to timelines and within budgets while always maintaining patient safety at the forefront of our strategies.
