MediSouq Pharmaceuticals PVT.

LTD

Date: 04-Aug-2022

To Whom It May Concern

Re: Mr. Tabrez Alam Shaikh Employment with MediSouq Pharmaceuticals PVT. LTD.

I confirm that Mr. Tabrez Alam Shaikh was employed as a full time Senior Data Manager for
MediSouq Pharmaceuticals PVT. LTD. and he had worked here from 02-Nov-2017 to 06-Nov-
2021at the following locations:

Designation City and Country Tenure (From DD/MM/YYYY – To

DD/MM/YYYY)
Senior Data Manager Mumbai, India From 02-Nov-2017 to 06-Nov-2021

MediSouq Pharmaceuticals is a global healthcare company based in Dubai that provides solutions
to address the evolving needs of patient worldwide. Main purpose of our company is to re-imagine
medicine to improve and extend people's lives. We use innovative science and technology to
address some of society's most challenging healthcare issues. We discover and develop
breakthrough treatments and find new ways to deliver them to as many people as possible. We also
aim to reward those who invest their money, time and ideas in our company.

Mr. Tabrez Alam Shaikh’s gross salary was INR: 5,16,000 per annum

Work schedule & hours of service: 9 :30 AM-7:00 PM (Mon-Fri), 46.5 hours per week.

Responsibilities & Duties:

1) Senior Data Manager (From 02-Nov-2017 to 06-Nov-2021)

 Executed and supervised 7 clinical studies of all the phases from setup to the closeout of a
clinical trial.
 Maintaining full understanding of clinical study protocol along with the other study
documents.
 MediSouq Pharmaceuticals PVT. LTD

 Creation and review of study setup documents like eCRF specifications (including data
capture screens and edit check specifications) and DVR specifications required to build a
clinical database to capture subject details.
 Designing of individual eCRF (Case report form) as per the user (clinical physician and
biostatisticians) requirement.
 Develop codes and test non-complex data management work products such as data entry
screens and database tables.
 Write test scripts and programs for database designing.
 Validation of edit checks and custom functions on different clinical databases as per the
study protocol.
 Coordinate with clinical research database analysts for the design, development, testing and
documentation of clinical trial database.
 Creation of project management plan at the time of study setup and updating the same on
regular interval along with client review.
 Creation of Data Transfer Agreement for different third party data Vendors.
 Creation of eCRF completion guidelines, in order to achieve 100% accuracy in data entry as
per the protocol.
 Performing third party data reconciliation between external vendor data and data in the
EDC database to ensure consistency.
 Ensuring ongoing data review/cleaning in on track during the study conduct and also
during prepare data cleaning timelines for database lock.
 Designing of back end checks, consistency checks and other reports needed for data review
by the study team members.
 Monitoring and helping in SAE reconciliation between safety and clinical database and
highlighting the issues to safety team to maintain a consistency between both the databases.
 Generation of quality and error free clinical data with no open queries before study
database lock.
 Preparation of study metric’s to inform about the status of clinical study to Leads, Project
Manager and clients in study calls.
 Managing a team to ensure high quality data is generated and milestones are achieved on
given time.

Sincerely,
For MediSouq Pharmaceuticals PVT. LTD,

Meer Rashid Ali

Director

Email Id:

Contact: