My past professional experience included organizational activities and other meeting logistics and preparing scientific reports as an outcome for scientific meetings and conferences. Prior to this I was working for a CRO where I was responsible for making regulatory submissions to the FDA for clinical trials sponsored by the Cancer Therapy Evaluation Program (CTEP) at the National Cancer Institute (NCI).To fill in the gap, acquired brief experience in a sales company managing the sales data of existing and prospective customers in the souvenir industry in the US. Before moving to the US, I worked for Syngene, a part of Biocon India Ltd on preparing, purifying and characterizing organic compounds(organic chemistry area).Specialties: Liaisoning between investigators & drug companies, regulatory affairs branch group & the Food and Drug Administration. Interacting between different branches in the Cancer Therapy Evaluation Program for example the RAB group, IDB group and Agreements Group, Database maintenance, Regulatory Documents Preparation