Coordinating and overseeing clinical trials, managing participant recruitment and enrollment, organizing study visits, ensuring protocol compliance, obtaining informed consent, tracking AEs, reporting SAEs, managing drug accountability procedures, eCRF and IXRS data entries, collaborating with interdisciplinary teams, participated in site initiation visits and site close-out visits and maintaining accurate records according to GCPTherapeutic Areas Of ExpertiseOncology: Non-small cell lung cancer, small cell lung cancer, muscle-invasive bladder cancerNephrology: Primary membranous nephropathyInfectious diseases: Transmission of InfluenzaHematology: Evaluation of severe or moderate Hemophilia A, Diffuse large B-Cell lymphomaOphthalmology: Uveitic macular edema, neovascular age-related macular degeneration

Directed manufacturing process and procedurs of Covid-19 test kits to achieve goal of first run capability. Assessed manufacturing processes and recommended improvements to increase productivity. Development of saliva Covid-19 test kits. Arranging staff shifts