Our quality focused approach commands continuous innovation and flexibility both at investigative sites and in-house. The O4 expert team create a customised site management programme for the successful delivery of the smallest of studies through to large complexed studies involving multiple sites with specific needs.
O4 research has strong and established relationships with its investigative sites across the UK and Ireland and the company’s close interaction with health and delivery processes enables new insights and solutions, practical support, site specific planning and the realisation of site specific goals. Our site committed controlled resource includes research nurses but also study co-ordinators. The O4 research study team provide;
- Training & Practical support & answering of study questions from sites
- Project Start-up services
- Site specific study action plans
- Patient recruitment specific strategies
- Clinical Trial Contracts
- Promotion of cross-site communication
- Budgets, contracts & payment management
- Performance of Actual Vs Plan
- Compliance monitoring
- Study Documentation/Systems
- Site specific Standard Operating Procedures
- Control of IMP
- Tracking and assistance with data query resolution
- Safety Reporting
Our study co-ordinators and research nurses have a clear focus on enabling a consolidated study duration and exceptional site performance including speed, reliability, productivity and data quality. By deploying such resource this affords greater efficiency, benefits and a balanced partnership between the clinical trial process and patient management.
Site management and logistic responsibility is therefore removed from the field based CRA allowing them to focus on the most critical aspects of their monitoring visit. The process of running a clinical trial from the very point at which the data are live when the patient and the study interface, right the way through to the production of a final report is managed with the highest quality standards and professional integrity.