Hi there,
I am qualified by Master of Science in Medicinal Chemistry and Master of Science in Clinical Research and Regulatory Affairs and also having more than 5 years of experience in the area of Clinical Research, Regulatory Affairs and Quality Assurance with the world's leading organization.
Till date, I have reviewed more than 100 of Global Clinical trial Protocols (Phase I to IV) and protocols for BA & BE trials.
I understand the importance of the task for which I am bidding which require 100% dedication and time management.