Amr Hisham

Zia Sun Egypt

• Senior Clinical Research SpecialistFull Time

  Sep 2020 - Present -4 yrs, 10 months

  Egypt , Cairo

  • Job Details:Reviewing Literature and ensure trial feasibility. Participate in writing and reviewing of study Protocol and Informed Consent form. Determining Study feasibility, budgeting and timeline. Monitoring study activities and adherence to study protocol, GCP and other regulations, tracking and reporting deviations, ensuring E-CRF good handling. Communication with Independent Ethics Committee (IEC), Regulatory authorities, sponsor and other stakeholders. Handling and maintain Electronic Data Capture (EDC) and E-CRF
• Clinical Research SpecialistFull Time

  Sep 2019 - Aug 2020 -11 months

  Egypt , Cairo

  • Job Details:Full Literature research about drugs and its active metabolites. Preparation of the trial master file of clinical study. Preparation of the study protocol. Responsible for clinical study steps conduction and monitoring.