Seeking an opportunity to contribute my expertise in clinical research, with over 9 years of experience in clinical research, data management, and international collaborative projects, while advancing my professional growth in a dynamic organization.
Ph.D. in Medical Parasitology with background in Immunology having extensive experience in clinical research, data analysis, and clinical trial management. Expertise in FDA regulatory compliance, clinical documentation, and data management systems (REDCap). Strong international project experience , worked with international researchers to facilitate cross-border research collaborations, contributed to research projects in India, Japan, and Qatar. Proficient in laboratory techniques (PCR, ELISA, Flow Cytometry), bioinformatics tools, and statistical software (GraphPad, SAS). Strong oral and written communication skills, with experience in technical writing, presentations, and cross-functional collaboration. Clinical research professional prepared to leverage extensive background in managing clinical trials and research operations. Adept at ensuring compliance with regulatory standards and enhancing study efficiency. Known for fostering collaborative team environments and flexibly adapting to changing needs. Skilled in patient management and protocol development.