Please, help is needed.

1b01i00The purpose of this letter is not only to describe my educational and professional background, but also to focus your attention on how motivated I am to start Master of Science program in Clinical Research Administration offered by the University of Liverpool.00 00I strongly believe that both my educational background and four years experience in the clinical research field make me a very good candidate for the program. 00 02i02b02br
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01b01i00I was graduated from York University (Toronto, Canada) in April 2004 with Bachelor of Science degree in Biology.00 00 00Two months after the graduation I joined Clinical Research training program offered by Kriger Research Center.00 00During this training I got familiar with GCPs (Good Clinical Practices), obtained essential knowledge about clinical research field and its key players: Sponsor, CRO (Clinical Research Organization), CRA (Clinical Research Associate)/Monitor, PI (Principal Investigator), CRC (Clinical Research Coordinator), etc. 00 02i02b02br
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01b01i00In 2004 my career in clinical research has began.00 00Endpoint Research Ltd offered me one year contract as Clinical Research Associate I.00 00My contract with Endpoint Research was extended once, so I spent two years with this company.00 00During these two years I learned a lot about clinical research.00 00I developed strong communication and leadership skills.00 00During these two years I have realized that clinical research is a field that I want to work in for the rest of my life.00 00With Endpoint Research Ltd I received a profound experience in a study site initiation, monitoring and close-out.00 00I managed and visited study sites to ensure site compliance with a protocol and regulatory obligations.00 00I learned how to document observations in reports and letters in a timely manner using approved business-writing standards.00 00I became a professional in all aspects of the clinical research monitoring: source document verification, validation of CRF entries, query resolution, investigational product accountability, reconciliation and collection of the investigational product, study site evaluation and selection, Serious Adverse Events (SAE) report and documentation. 00 00 00 00 00 00 00 02i02b02br
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01b01i00In August 2006 I signed a 6 months contract as Clinical Research Quality Manager with the small SMO (Site Management Organization) called Trial Management Group Inc.00 00My role was to review and update company’s SOPs (Standard Operating Procedures).00 00I also developed training methods for PIs and CRCs and trained them on GCP conduct and SOPs.00 00I conducted QA visits and special visits to assist sites to prepare for FDA audits and other regulatory bodies’ inspections.02i02b02br
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01b01i00In June 2007 I joined The Canadian Heart Research Center (The CHRC) as a Senior Clinical Research Coordinator.00 00I found this position very useful for my development in the clinical research field because it gave me a chance to learn about clinical research from the other side.00 00As CRA I new research from the side of sponsors (pharmaceutical or biotechnological companies), as a CRC I learned clinical research from the side of Principal Investigator.00 02i02b02br
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01b01i00I strongly believe that Master of Science degree will be a very strong and necessary addition to my career path.00 00I see myself in the managerial position within clinical research field; however I think that I have to prepare myself to move forward to my goal.00 00There is no doubt that Master of Science in Clinical Research Administration with the University of Liverpool is the right choice for me.00 00I am very motivated to start this program.00 02i02b02br
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01b01i00Steady and successful personal and professional development can not be achieved without growing up educationally.00 00Therefore, it is very important for me join the University of Liverpool.00 00 02i02b02br
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00George Tabulov0-