Clinical Operations and Project Management

Greenline Clinical Research delivers unmatched experience as the North America-Region leading CRO with expert teams and deep local regulatory knowledge.

The streamlined and integrated clinical trial services are delivered by teams of professionals with strong industry and therapeutic area expertise across all phases of clinical development. The teams also have established relationships with trial sites, key opinion leaders and Principal Investigators resulting in rapid and effective trial start-up, patient recruitment and site selection.

A full range of Project Management services

• Feasibility assessment and site selection
• Protocol development & CRF design
• Patient recruitment strategies
• Ethics Committee and Regulatory submissions
• Project management and monitoring for Phase I–IV trials
• Full biometrics services, including randomization and IWRS services
• Local sponsorship
• Third party vendor management
• Medical, technical and CSR writing

Site Management (SMO) activities

Greenline Clinical Research's Site Management Organization (SMO) service provides highly qualified and experienced Study Coordinators (SCs) and Site Management Associates (SMAs) to help support both principal investigators and sponsors.