Mostafa Kaboa

Experience

• 

  Salah el din pharmacy

  May 2015 - Nov 2016

  Community Pharmacist
• 

  Zi Diligence

  Aug 2016 - Oct 2020

  Developing techniques for the analysis of drug products and chemicals; using a range of analyticaltechniques, instrumentation and software.performing sample pre-treatment and protein precipitation and Liquid Liquid Extraction (LLE) of plasmasamples. - Validating methods and equipment.Operating HPLC (Agilant 1260 ) , UPLC Waters Aquity H class , Mass spectroscopy API sciex 4000 and APIsciex 4500.

  • Clinical Research Specialist

    Aug 2019 - Oct 2020

  • Senior Analyst

    Feb 2018 - Aug 2019

  • In vivo and Invitro analyst

    Aug 2016 - Jan 2018
• 

  Pharma Guide Egypt

  Oct 2020 - now

  1-development of clinical trial protocols; participates in the development of the overall clinical plan, drafts protocols, collaborates on statistical analysis plans, and coordinates the protocol review and approval process, to include submissions to regulatory agencies.2-Prepare and Reviews on-site files and records, case report forms, and source documents for completeness, accuracy, consistency, and compliance; identifies deficiencies and discrepancies, and provides remedial training and/or initiates corrective action as required. Show less 1-Creation and Maintenance of study master file.2-Assistant in informed consent procedure3- Organization during screening and enrolment of study participants with PI.4-scheduling study visits for study participants and organization of the investigator site file.5- Reviewing and reporting adverse events and serious adverse events according to the study protocol, standard operating procedures and applicable regulatory requirements.6- Reviewing subjects study data for accuracy and consistency.7- Collection accurate and verifiable data to complete and file case report forms in accordance with good clinical practice8- Training study staff on SOPs and study protocol9-Delivery of Bio samples to laboratory. Show less 1-Development of clinical study protocol.2-Case Report form (CRF) design, development and completion.3-Calcualtion of Pharmacokinetics parameter ( Phoenix winnonlin software and R studio). 4-Statistical analysis (ANOVA and confidence interval-CI ) for clinical studies concerning pharmacokinetics parameters using ( Phoenix winnonlin software and SAS software) 5-Randamization plan for study using R studio.6-Samle size calculation and calculation of power post study analysis using R.7-Prepration and reviewing of final clinical study reports. Show less

  • Clinical Research and Data management Manager

    Oct 2021 - now

  • Clinical Research specialist

    Oct 2020 - Oct 2021

  • Medical writer , Biostatistician and data management

    Oct 2020 - Oct 2021