Vendor Management & Governance
When engaging multiple providers in a study, all can be project-managed by one governance officer under one consolidated contract, if preferred.
Additional Services
- Full and complete Medical Writing
- Clinical Site Agreement negotiations and management
- Patient Recruitment and Retention
- Regulatory Strategy
- Audit – GCP Preparedness
- Printing and Fulfillment for Clinical Research
- Responsible for the day-to-day execution of a clinical trial
- Vendor management (EDC, IRT, Rating/assessments, ePRO/eCOA, Imaging, Central Safety and Specialty labs etc.)
- CRO management
- Site management
- Budget management
- Site feasibility
- Clinical Development Planning
