- Protocol and trial development and management
- Grant submission
- Submission to ethics committee (IRB)
- Patients recruitment and follow up
- Biological samples processing and storing
- Data entry forms – paper and electronic (including development and maintenance of electronic case report form according to regulations)
- Reporting of adverse events and serious adverse events and SUSARS according to CTCAE guidelines
- Data extraction from the databases at Soroka and Clalit Health Services
- Statistical programming and analysis
- Medical writing such as protocol, scientific reports and publications
We collaborate with physicians, nurses, and medical students from both medical and paramedical fields to ensure that research is conducted in the most effective and safe manner for patients and the success of the research.