As a clinical research protocol extractor and digitizer, I have over seven years of experience in the clinical research domain, working on phase I to IV trials with diverse indications. I hold an ACRP certification in clinical research and a master's degree in pharmaceutics, which enable me to apply my knowledge and skills to design, write, and digitize effective and compliant protocols. In my most recent role at Atos Syntel, I was responsible for extracting and digitizing protocol-related data from clinical research studies, using software programs and tools. I also managed and monitored sites, ensured quality and compliance, and mitigated risks. Additionally, I developed and delivered training and presentations to enhance collaboration and teamwork within the organization. My mission is to provide strategic solutions to clinical challenges and deliver high-quality clinical services.