As the Founding Director of Operations, I took on the pivotal role of orchestrating the inception and execution of our laboratory diagnostic procedures. In this capacity, I effectively oversaw a team comprising five key individuals, leading the charge in operational management for a diverse clientele encompassing patients across all 50 states. Presently, our organization has transitioned its focus towards clinical trials, and we are actively working with clients to streamline clinical trial operations.

I led studies focused on the introduction of new pharmaceutical products. This involved coordinating the schedules of patients, therapists, and doctors, all while strictly adhering to protocol guidelines.• Swiftly advanced from Research Assistant to Research Coordinator within just 6 months.• Successfully completed training in CITI, Blood-borne Pathogen, and CPR certification courses.• Handled daily query resolution and data maintenance across multiple programs, including IMedidata, In-Form, Media, Encapsia, TrialMaster, and AiCure.• Managed and supervised up to 8 concurrent clinical research studies, overseeing everything from subject consent to screening and treatment completion.• Organized meetings to educate staff about new clinical trials.• Crafted source documents for all clinical research studies, optimizing the collection of both quantitative and qualitative data during each subject's visits.• Ensured the meticulous organization of study documentation, prepared lab kits according to study protocols, and maintained all patient medical records.• Conducted visits with pharmaceutical Clinical Research Associates (Monitors).• Consistently met deadlines and surpassed expectations for timely data collection and submission.

Co-Author of, “Change detection in complex auditory scenes is predicted by auditory memory, but not years of musical training.”