Skilled Clinical Research Coordinator with experience working with Contract Research Organizations (CROs), Pharmaceutical companies and expertise in gathering and analyzing data for clinical trials. Proficient and skilled in defining protocols and validating protocols in clinical studies. Ability to handle and maintain trials responsibility during the data management cycle. Advance EDC system skill set with expertise in database design and protocol objectives. Knowledgeable in GCP, FDAstandards/regulations, and therapeutic indications. Experienced in managing and maintaining multiple studies, study evaluations, study initiations, and close out in compliance with GCP and hospitals SOPs.Versed in the creation of SOPs and ensuring study integrity. Experienced with applying GCP and ICH regulatory guidelines. Training and awareness in Diverse, Equity, and Inclusion, team player, resourceful colleague, consistently meet/exceed expectations.