- Completion and return of CRF’s
- Data Queries
- Support monitoring visits, audits and inspections
- Arranging and collecting research patient’s notes for own and other research personnel’s use
- Liaising with other health professionals as required
- Maintaining / allocating appropriate copies of research documentation inpatient hospital & research records
- Maintenance of study files to ICH GCP standards
- Support lead study clinician and other research professionals in-
- Documentation of adverse events in the data source
- Investigator/study file set up and management
- Preparation of paperwork for Ethics committee and R&D approval
- Appointing new study coordinators
- Providing training and evaluation of study coordinators
- Selection of trial to be conducted (wherever applicable)
- Review of source data and CRFs before monitoring.
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