• Protocol and trial development, and management
  • Grant submission
  • Submissions to local ethics committee (LEC/IRB)
  • Participant recruitment and follow up
  • Biological samples collection, processing and storing
  • Data entry forms – paper and electronic (including development and maintenance of electronic case report forms (CFRs) according to regulations)
  • Reporting of adverse events (AE), serious adverse events (SAE) and SUSARS according to CTCAE guidelines
  • Data extraction from the databases of Israel's largest HMO (Clalit Health Services) and SUMC
  • Statistical programming and analysis
  • Medical writing such as protocol, scientific reports and publications

 

We collaborate with physicians, nurses, medical students and people from both medical and paramedical fields to ensure that research is conducted in the most effective and safe manner for patients alongside the success of the research.