This document is a resume for Shaymaa Mohammed Mohammed Youssef El-Awady. It summarizes her personal and contact information, education history including a Master's degree in Clinical Pharmacy from Ain Shams University, work experience in clinical pharmacy and clinical research, skills and qualifications, training and certifications, publications and presentations, membership and references. The resume demonstrates over 15 years of experience in clinical pharmacy, clinical research, and pharmaceutical quality and regulatory affairs.

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Name : Shaymaa Mohammed Mohammed Youssef El-Awady
Date of Birth : 09 / 09 / 1979
Place of Birth : Cairo, Egypt
Address : 233, beside Akhnaton College, fifth settlement, New Cairo, Egypt.
Marital Status : Married
Religion : Muslim
Nationality : Egyptian
Phone : + 202 25607352 // + 202 22742694 (Home)
Mobile phone : +201021056599 //+201005795179
E-mail : shaymaaelawady@gmail.com
LinkedIn : https://eg.linkedin.com/in/shaymaa-el-awady-m-sc-b42b4469
November 2009 – December 2014: Master degree in Clinical pharmacy
Faculty of Pharmacy, Ain Shams University with a research title “EVALUATION OF THE
PROPHYLACTIC ANTIBIOTIC POLICIES OF CARDIAC SURGERY IN A UNIVERSITY
TEACHING HOSPITAL”, had a very good grade in the pre-master’s studies, and the Practical work
was carried out at the cardiothoracic surgery department, El-Demerdash teaching Hospital, in Ain
Shams University.
November 2007 – November 2008: Clinical Pharmacy Diploma
Faculty of Pharmacy, Ain Shams University (Excellent).
September 1996 – May 2001: Bachelor degree in pharmaceutical sciences
Faculty of Pharmacy, Ain Shams University (Accumulated grade: very good)
1. Very good command in English Language: Reading, writing and speaking.
2. Fair command in French Language: Reading, writing and speaking.

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1. Microsoft Windows
2. Microsoft Word, Excel and power point
3. SPSS for statistics
4. Redcap for data management
5. Internet
1. "ESFJ" personality in the MPTI - Personality test results.
2. Dynamic, self-motivated and hard worker.
3. Ability to work under pressure.
4. Ability to express ideas concepts.
5. Good communications skills.
6. Ability to work in a team-work environment.
1. Training in Hazem pharmacy, Nasr City (Two years).
2. Training in Tarek pharmacy, Nasr City (Two years).
4. Part-timer translator of medical pamphlets in HBC (Heliopolis Business Center)
(6/2001-till now).
5. Shift manager at Khalid Ibn El- walid pharmacy (5/2002-6/2005).
6. Working in ACAPI Pharmaceutical Company, Badr city (07 / 2001- 5 / 2002):
6.1) Work in Registration Department.
(a) Preparation of registration files of the new drugs.
(b) Follow up of the registration files in MINISTRY OF HEALTH.
(c) Contact with different department in the factory to acquire and arrange the
needed information for the registration process
6.2) work as Production Pharmacist in solid dosage form department.
(a) Supervision of preparation process.
(b) Supervision of compression process and /or filling process (capsules)
(c) Supervision of packaging process.
(d) Complete awareness about principles of Good Manufacturing Practice (GMP).
(e) Good knowledge of the main requirements of the International Organization for
Standardization (ISO 9000 & ISO 14001).
7. Working in Ain Shams University Hospitals (5 / 2002 –11/2013):
7.1) Work as a pharmacist in drug stores.
a. Dealing (Receiving & Dispensing) with the drugs come to the stores
especially (cytotoxic drugs).
b. Preparation of the Tenders made by the hospital.
c. Dealing with different parts of the hospital to arrange their needs
from the drugs.

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7.2) Work in the drug supply department
a. Dealing with different parts of the hospital by arranging their needs from
drugs and managing drug orders
b. Follow up drug delivery from distribution companies and receiving of drugs
by pharmacists of drug store.
c. Responsible for preparing tenders and their execution (Injectable drug
products, Injectable antibiotics, medical gases).
8. Working as Clinical Research Lead in Natural Wellness Egypt scientific
office (8 / 2013 –till now):
Natural Wellness Industries Sdn Bhd is one of Malaysia's fastest growing nutraceutical and
Cosmeceutical Company
a. Management and monitoring clinical research part (Phase I, II and III) of the Malaysian
Ministry of Agriculture (MOA) Grant on six herbal products.
b. On August 2014, finalizing and submitting Phase I clinical trial reports for the project three
products.
c. On September 2014, preparing with the CRO for Phase II clinical trial of the project three
products.
d. Designing drug labels and setting randomization according to randomization plan decided.
e. On November 2015, issuing of phase II final reports for the three products of the project.
f. Preparing the Interim reports for the running trials and presentations for the new research
projects' products.
g. Requesting for proposals from different CROs and communication with their managers for
CRO selection by Natural Wellness.
h. Acting as the main line of communication between the sponsor and the investigator.
i. Verifying that the investigator has adequate qualifications and resources and remain
adequate throughout the trial period.
j. Verifying, for the investigational product.
k. Verifying that the investigator follows the approved protocol and all approved
amendment(s), if any.
l. Verifying that written informed consent was obtained before each subject's participation in
the trial.
m. Ensuring that the investigator receives the current Investigator's Brochure, all documents,
and all trial supplies needed to conduct the trial properly and to comply with the applicable
regulatory requirement(s).
n. Ensuring that the investigator and the investigator's trial staff are adequately informed about
the trial.
o. Verifying that the investigator and the investigator's trial staff are performing the specified
trial functions, in accordance with the protocol and any other written agreement between the
sponsor and the investigator.
p. Verifying that the investigator is enrolling only eligible subjects.
q. Reporting the subject recruitment rate.
r. Verifying that source documents and other trial records are accurate, complete, kept up-to-
date and maintained.

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s. Verifying that the investigator provides all the required reports, notifications, applications,
and submissions, and that these documents are accurate, complete, timely, legible, dated,
and identify the trial.
t. Checking the accuracy and completeness of the CRF entries, source documents and other
trial-related records against each other.
u. Informing the investigator of any CRF entry error, omission, or illegibility and ensuring that
appropriate corrections, additions, or deletions are made, dated and initialed by the
investigator or by a member of the investigator's trial staff who is authorized to initial CRF
changes for the investigator.
v. Determining whether all adverse events (AEs) are appropriately reported within the time
periods required by GCP, the protocol, the IRB/IEC, the sponsor, and the applicable
regulatory requirement(s).
w. Determining whether the investigator is maintaining essential documents.
x. Communicating deviations from the protocol, SOPs, GCP, and the applicable regulatory
requirements to the investigator and taking appropriate action
6. Part-timer transcriptionist at Nagy Research CRO (3/2014-till now)
Had a poster presentation at “The 17 th
Scientific Congress of the Association of College of
Pharmacy in the Arab World (from 14th
to 16th
October 2014)” with Abstract entitled
“EVALUATION OF THE PROPHYLACTIC ANTIBIOTIC POLICIES OF CARDIAC SURGERY
IN A UNIVERSITY TEACHING HOSPITAL”
Had participated in The First MSA Clinical Pharmacy Scientific Day on 27th
April, 2013 at
faculty of pharmacy, October University for Modern Sciences and Arts (MSA University).
Had participated in the scientific day on Chronic Myeloid Leukemia, which was held at the
Intercontinental City Stars, Heliopolis, Cairo, on Monday, October 4th
, 2010.
Had a paper publication with the title of "EVALUATION OF THE PROPHYLACTIC ANTIBIOTIC
POLICIES OF CARDIAC SURGERY IN A UNIVERSITY TEACHING HOSPITAL” at "The
American Journal for Pharmatech" Journal in December 2014 issue.

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Summer 2002:
ICS courses of Ms-Excel 2000 and Ms-Access 2000 at Arab El Mohammady Library Training
Center.
March 2013 – April 2013:
"Statistics for Clinicians" course at the cardiothoracic surgery department, El-Demerdash
Teaching Hospital, Ain Shams University.
October 2013-February 2014:
Successfully completed and received a 99% grade in "Fundamentals of Clinical Trials" online
course from Harvard University, edx HarvardX.
December 2013 –January 2014:
Attending "We are One Team"," Time Management", "Communication Skills "And "Business
Writing" courses at LEAD center for training and development.
February 2014 – March 2014:
Successfully passed GCP web‐based training course designed and developed by INFONITICA
covering all aspects of Good Clinical Practice as laid down in the International Committee on
Harmonization on Guidelines, Certificate No: 322932640601.
February 2014-March 2014:
Successfully completed and received a 96.7% grade in "Design and Interpretation of Clinical
Trials" online course from the Johns Hopkins University, Coursera.
May 2014-July 2014:
Successfully completed Vanderbilt University Online offering gaining a Statement of
Accomplishment WITH DISTINCTION in "Data Management for Clinical Research" online course
from the Vanderbilt University, Coursera.
May2014-June2014:
Attending a training at GRC (Genuine Research Center) in the bioequivalence department, clinical
t trials department, and the Laboratory.
May 2014:
Attending a workshop entitled "From Protocol to Publisher: An Original Article For A Medical
Journal" organized by Egyptian Society of Cardiology (EgSC) in collaboration with Egyptian
Clinical Research Team (ECRT) held at Egyptian Heart House, Dokki, Giza, Egypt.
October 2014-March 2015
Attending NIH course offered by The United States National Institutes of Health (NIH) hosted
by EAMTAR entitled "Introduction to the Principles and Practice of Clinical Research (IPPCR)" a
comprehensive course about Clinical research at the NIH headquarters in the US and
EAMTAR hosted this course as a registered remote site making it available in Egypt.
Successful completed and received 97%

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Member in the Egyptian Clinical Research Team (ECRT), a group belongs to the Egyptian Society
of Cardiology (EgSC) at Egyptian Heart House, Dokki, Giza, Egypt.
1. Dr. Mohsen Fathallah
CEO & Managing Director at GRC, Egypt.
Mobile: +2/01001467860
mohsen.fathallah@grc-me.com
2. Dr. Silvana Aiziz
Ain shams university hospitals pharmacy department Manager
Mobile: 01005198715
silvana.aziz@hotmail.com
3. Dr. Basemah Fawzy
Fellow Intensive Care and Echocardiography
Ain shams university hospitals cardiothoracic surgery department.
Mobile: +2/01068863991
basmhfawzy@gmail.com
4. Dr. Manal Hamed El-hamamsy
Professor of Clinical Pharmacy, Faculty of Pharmacy, Ain Shams University
Mobile: +2/01005257416
m_elhamamsy@hotmail.com
As a young pharmacist, I am looking for a challenging position that will take full
advantage of my education, training, and experience and acquired skills. In addition,
this position should give me the opportunity to improve my knowledge, and give me
the experience, which allows me to achieve my professional goals and put me on the
competition level, as well as to positively influence organization operation, performance
and profitability.