Ahmed Abou Elyazid Email & Phone Number

Cairo, Egypt

Cairo, Egypt

Cairo, Cairo, Egypt

- working with team members from scratch on creating medical and pharmaceutical materials used by HCPs or the public, based on referenced scientific facts and latest clinical trials with an attractive and sample layout.

Cairo, Egypt

• Monitoring phase 2 clinical trials involving monitoring visits to the trial sites.• Source data verification.• Informed consent form review, case report form review, investigational drug accountability, and adverse event review.• Writing visit reports, filing, and collecting trial documentation and reports.• Preparation of submission packages and submission to local ethics committees and regulatory authorities.• Worked closely with medical writing to review protocols… Show more • Monitoring phase 2 clinical trials involving monitoring visits to the trial sites.• Source data verification.• Informed consent form review, case report form review, investigational drug accountability, and adverse event review.• Writing visit reports, filing, and collecting trial documentation and reports.• Preparation of submission packages and submission to local ethics committees and regulatory authorities.• Worked closely with medical writing to review protocols, ICFs, and CRFs.• Identifying/selecting an investigator who will be responsible for the conduct of the trial at the trial site.• Setting up the trial sites, which includes ensuring each center has the trial materials.•Evaluated electronic data capturing systems for adherence to guidelines.• Worked closely with data management and site teams to resolve discrepancies.• Assessed adherence to procedures, practices, and all applicable regulatory requirements. Show less

Cairo, Egypt

• Coordinate studies from start-up through closeout.• Determine eligibility of and gather consent from study participants according to protocol. • Assist in developing recruitment strategies.• Coordinate collection of study specimens and processing.• Collect and manage patient and laboratory data for clinical research projects.• Manage research project databases and other study-related documents. • Complete study documents/case report… Show more • Coordinate studies from start-up through closeout.• Determine eligibility of and gather consent from study participants according to protocol. • Assist in developing recruitment strategies.• Coordinate collection of study specimens and processing.• Collect and manage patient and laboratory data for clinical research projects.• Manage research project databases and other study-related documents. • Complete study documents/case report forms.• Ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents. • Participate in monitor visits and regulatory audits.• Develop and implement databases, data collection systems, data analytics and other strategies that optimize statistical efficiency and quality• Interpret data, analyze results using statistical techniques, and provide ongoing reports. Show less

Egypt

• Handling with experimental animals (rats)• Blood sampling and termination for rats• Understanding OECD guidelines for Toxicity Studies• Reading ISO 9001:2008• Filter and “clean” data by reviewing computer reports, printouts, and performance indicators to locate and correct code problems• Statistical packages analysis using datasets (Excel, SPSS)• Pre-clinical research, statistical, data validation &reporting. • Design case forms and other recording… Show more • Handling with experimental animals (rats)• Blood sampling and termination for rats• Understanding OECD guidelines for Toxicity Studies• Reading ISO 9001:2008• Filter and “clean” data by reviewing computer reports, printouts, and performance indicators to locate and correct code problems• Statistical packages analysis using datasets (Excel, SPSS)• Pre-clinical research, statistical, data validation &reporting. • Design case forms and other recording measures, determine appropriate validation tests, specifically define data collection methods and measurements, develop databases and other computer programs to explore and detail research findings and help to prepare and present data to stakeholders and other interested parties. Show less

Master'S Degree, Computer Science

Diploma Computer Science, Computer Science, 2.8

Bachelor'S Degree, Chemistry And Zoology

Premaster, Cell/Cellular Biology And Histology

Master degree in bioinformatic cytogenetic

Continuing Medical Education (Cme), Clinical Management, 19 Cme Credit