Clinical Pharmacist
Aya Specialist Medical Hospital (Maternity&Children)-Jeddah-KSA July 2016- 2017
 Evaluate all Medicare coverage requirement requests and ensure compliance to all clinical
procedure and coordinate with pharmacy and medical staff to perform regular
interventions according to present drugs.
 Perform regular evaluation on all usage and dosage and ensure absence of all reactions and
assist all patients with assessment of patient orders and prescription infusion and ensure
adherence to all laws and regulations.
 Gather, maintain and analyze all laboratory data and record all required patient
information and make recommendations to change dosage if required.
 Administer and complete all pharmacy care plans and perform reconciliation of all
medication and supervise all sterile mixing processes.
 Review all medications and equipments and ensure accuracy and effective functioning and
manage all communication with physicians and patients and assist to resolve all patients
within required timeframe.
 Maintain record of all medication for patients and ensure absence of all discrepancies and
analyze all side effects and drug interactions.
 Coordinate with all medical case managers and evaluate all high risk members to prevent
all risks and participate in all patient associated meetings.
 Prepare all clinical documents and participate in all on call activities for pharmacy and
evaluate all pharmacy claim data and identify all clinical savings.
 Attend all therapeutic and pharmacy committee meetings.
Pharmacist
IMC (International Medical Center)-Egypt Feb 2015-Aug 2015
Prepares medications by reviewing and interpreting physician orders; detecting therapeutic
incompatibilities. Dispenses medications by compounding, packaging, and labelling
pharmaceuticals. Controls medications by monitoring drug therapies; advising interventions.
CTA (Clinical Trials Assistant)
Dataclin (Clinical datamanagement)-Egypt July2014-Jan 2015
 Maintain and update all clinical system and monitor all performance within timeframe and
prepare all documents for operating procedures and evaluate all documents.
 Maintain effective receipt of all regulation documents from study site.
 Assist to ship all drugs and resolve all issues in financial documents and prepare reports for all
invoices and maintain inventory of all non-drug clinical supplies.
 Gather and monitor all financial files for SOP and plan various study meetings and participate in
associate meetings to provide support and documents all clinical study reports electronically.
 Coordinate with various study sites and evaluate same on periodic basis to ensure accuracy in
same and prepare and distribute all clinical trial supplies and maintain same.