The clinical research associate (CRA) performs monitoring tasks by reviewing subjects’ medical records, etc. Also, it is important for the CRA to share the information with physicians, study coordinator, and the study sponsor in a timely manner.
In order to carry out appropriate monitoring, it is essential to receive accurate information in a timely manner while maintaining good communication.
In the case of clinical trials commissioned by pharmaceutical companies, SRL Medisearch performs various application processes, coordinates with investigators, the study coordinators, and other site personnel, collects case report forms, provides safety information, etc. in a rapid and reliable manner, and in accordance with GCP, protocols, and SOPs.
- Phase I, II, and III clinical trials
- Bioequivalence studies
- Post-marketing study
- Investigator initiated clinical trials
Tasks are allocated within the monitoring team. This allows CRAs to stay focused on monitoring activities, enabling high-quality and efficient monitoring activities.
- Phase I, II, III, and IV clinical trials, and Investigator initiated clinical trials