Upfront planning results in fewer study delays and errors, assuring you receive high-quality study outcomes. Our clinical trial management philosophy supports all aspects of your early clinical trials cost effectively with clear roles and responsibilities.
Whether using our clinical research centers or our qualified external sites, your project manager is a key resource in managing your study. These seasoned professionals, with relevant scientific and therapeutic expertise, serve as your central contact throughout the entire process.
Let us help you:
- Develop the project plan and timeline
- Start-up activities and study initiation
- Oversee study conduct and clinical monitoring
- Manage data support teams from protocol development to clinical study report
- Maintain and report pharmacometrics deliverables
- Select and manage vendors
An eye for detail. Precision delivery.
It takes special people to monitor clinical trials. Individuals with flexibility to hop on a plane at a moment’s notice, with an eye for detail and a broad understanding of regulations and Good Clinical Practices. Our independent clinical trial monitors ensure your study complies with multiple regulations. We protect the rights of subjects and ensure study data are accurate, complete and verifiable from source data.
You have access to a network of CRAs experienced in monitoring early phase trials from first-in-human through PoC, in settings including our clinical research units (CRUs), external CRUs, hospitals, specialized research centers and medical practice settings.