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Health Informatics 
Rutgers, The State University of New Jersey 
65 Bergen Street, Room 171 
Newark, NJ 07101-1709 
shrp.rutgers.edu/dept/biopharma/index.html 
biopharma@shrp.rutgers.edu 
p. 973-972-6482/8444 
f. 973-972-7228 
May 12, 2014 
Re: Samreen Jamil 
To: Hiring Manager 
MS in Clinical Trial Sciences 
An Industry and University Collaboration 
It is with extreme pleasure that I recommend Samreen Jamil for a position at Merck as a 
summer intern. I have known Samreen since the beginning of Fall 2013 semester when she 
entered our Masters of Science Program in Clinical Trial Sciences. She is articulate, writes well 
and is an all around excellent student. 
This is a very rigorous program and Samreen has proven herself well. She has taken Overview 
of Disease Process (Pathophysiology), Clinical Pharmacology, and Clinical Trials Overview. 
She is very familiar with the process of drug development; human subjects protection, research 
design, as well as clinical pharmacology. I have attached a copy of our brochure so you can 
learn a little more about our program and culture surrounding our program. If you have any 
further questions, please feel free to contact me. 
Best Regards 
Barbara Gladson, PhD 
Director, Rutgers Biopharma Educational Initiative.

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Recommendation letter

  • 1. Health Informatics Rutgers, The State University of New Jersey 65 Bergen Street, Room 171 Newark, NJ 07101-1709 shrp.rutgers.edu/dept/biopharma/index.html biopharma@shrp.rutgers.edu p. 973-972-6482/8444 f. 973-972-7228 May 12, 2014 Re: Samreen Jamil To: Hiring Manager MS in Clinical Trial Sciences An Industry and University Collaboration It is with extreme pleasure that I recommend Samreen Jamil for a position at Merck as a summer intern. I have known Samreen since the beginning of Fall 2013 semester when she entered our Masters of Science Program in Clinical Trial Sciences. She is articulate, writes well and is an all around excellent student. This is a very rigorous program and Samreen has proven herself well. She has taken Overview of Disease Process (Pathophysiology), Clinical Pharmacology, and Clinical Trials Overview. She is very familiar with the process of drug development; human subjects protection, research design, as well as clinical pharmacology. I have attached a copy of our brochure so you can learn a little more about our program and culture surrounding our program. If you have any further questions, please feel free to contact me. Best Regards Barbara Gladson, PhD Director, Rutgers Biopharma Educational Initiative.