Ms. Jayashree Mathapati

With a Bachelor of Engineering in Biotechnology and over three years of experience as a Clinical Research Coordinator, I have honed my skills in managing clinical trials, ensuring compliance with protocols, and coordinating with cross-functional teams. I am proficient in data management, patient recruitment, regulatory documentation, and research study documentation.

My expertise in clinical research has led me to take on responsibilities within an Ethics Committee, where I managed the organization of meetings, scheduling, and planning, as well as the documentation and record keeping. My role also involved compliance monitoring, research and analysis, and communication about guidelines and decisions. Additionally, I developed education and training programs to ensure all relevant parties were well-informed and prepared with the necessary materials.

Currently serving as a Research Officer, my responsibilities include assisting in the documentation processes of the company, drafting protocols, case report forms, and informed consent forms. I also prepare final documents post-review by the Director, download research articles, handle external correspondences for publication, and manage any other relevant documentation work.