- Assisted in medical and cosmetic dermatology procedures including excisions, skin cancer screenings, injectables administration- Managed and led teams through fast-paced, high-pressure situations on a daily basis at a high-volume award-winning luxury dermatology practice- Anticipated and fielded general medical and aesthetic patient questions- Invited to serve as the Study Coordinator and IP Reconstituer for an FDA Phase III Clinical Study - Utilized the Electronic Medical Record, and other data software to create patient notes, send prescriptions, execute insurance prior authorizations, and monitor lab results- Oversaw medical billing and coding for patient medical insurance claims- Implemented tactical process improvements to increase organizational efficiency and speed

- Published two research papers in scientific journals (Schizophrenia Bulletin and Schizophrenia Research) and assisted in conducting and writing papers for over 5 additional studies- Managed a team of 8 researchers, oversaw data collection and integrity, anded 30+ Clinical Assessment Interviews of patients with schizophrenia to inform research objectives- Ensured compliance through a perfunctory audit from the IRB. Prepared necessary clinical regulatory documents and coordinated closely with IRB employees to understand and adhere to clinical guidelines- Developed the experimental design to screen at-risk groups for early signs of schizophrenia- Conducted extensive literature reviews for potential research studies