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Sponsoring Institutions
Our staff provides the expertise necessary to ensure smooth and efficient implementation of clinical trials. The benefits that the CRC can offer to Sponsoring Institutions include:
- Timely approval of the study by the Ethics Committee
- Timely contract and budget negotiation leading to rapid study initiation
- Efficient study coordination and monitoring from study initiation to study termination
- GCP training of personnel
- Quality Assurance
- Large pool of available volunteer/patients
- Protocol development
The outcome of any clinical trial depends upon the accurate and timely gathering of research data. At the CRC, each clinical trial is coordinated by expert Study Coordinators who provide the highest standards in clinical research.
Study Coordinators
Study Coordinators provide day-to-day support to the CRC personnel and work with sponsors for a timely initiation of the study. Study Coordinators are an invaluable resource to guarantee high quality training of the staff in Good Clinical Practices (GCP) and Standard Operating Procedures (SOP). Our Study Coordinators also contribute to the development of innovative trial-management strategies to maximize efficiency.
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