Maurice Okello Email & Phone Number

A clinical research professional with 5 years' experience, well-versed with clinical trials regulations such as ICH-GCP guidelines, local regulatory authority and IRB approval requirements, study start-up, safety monitoring, risk-based monitoring, data quality monitoring, source data review and verification, drug development process, the roles and responsibilities of sponsors, investigators, and monitors, the operations of the ethical review committees and regulatory authorities, planning and conducting of investigator meetings and site visits, the management of essential documents and trial master files,reporting of protocol deviations and adverse events, and the preparation for audits and inspections.Experienced working in phase III, IV trials and Drug re-purposing studies. Also worked in and internally monitored pilot studies on Maternal and Child Health, Malnutrition and HIV.