Alaa Shahbar

Experience

• 

  Roche

  Oct 2010 - Jan 2012

  Clinical Research Associate

   Perform site visibility and initiation visit to train trial medical team on data entering e-RDC program, and monitoring steps. Perform monitoring visit through:I. Verify the entered data in e-CRF.II. Help in solving discrepancies and inquires in e-CRF.III. Inspect clinical trial drug storage place, quantities , temperature.IV. Drug accountabilityV. Insure the investigator site file contains all the essential documents and correspondence: Ethics committee and Saudi FDA Approvals, trail agreement ,protocol, investigator brochure, informed consent form , Authorization form, training records (insure the trial team got the training on GCP guideline, safety and on entering data system), financial disclosure, drug onsite destruction. Update Clinical Trial Management System (CTMS). Prepare and Submit the Packages to SFDA to obtain preliminary approval for conducting clinical trials and clearing the Investigational Medication product (IMP) from Saudi Custom. Prepare and submit the Packages to Ethics Committee to get on hospital approval for conducting the clinical study. Show less

• 

  Umm Al-Qura University

  Jan 2012 - May 2018

  Teaching Assistant

  - Teach and supervise students during internship- Teach and assist with therapeutic classes- Assist with practical therapeutic sessions

• 

  MCPHS Univeraity

  Aug 2016 - now

  Registered pharmacist in USA
• 

  King Abdullah Medical Complex - Jeddah

  Jan 2017 - Jan 2018

  Pharmacist

  perform outpatient, inpatient, IV and TPN services

• 

  King Abdullah Medical City (KAMC) - Jeddah

  Oct 2018 - Sept 2020

  PGY-1

  Pharmacy resedency program