Professional with 15 years of experience in planning and performing phase I, II, III and IV clinical research in different therapeutic areas:Ophthalmology: glaucomaNervous system: insomnia, headache, epilepsy, post-traumatic stressCardiovascular: hypertension and dyslipidemiaGenitourinary: Prostatic hyperplasiaRespiratory: asthma, colds, colds and fluPain: low back pain, Tooth extractionGastroenterology: diarrheaDermatology: androgenetic alopecia, inflammatory skin diseaseOtorhinolaryngology: otitis externaThroughout my career, I played many roles in the clinical trial area for large pharmaceutical companies, including the development of clinical protocols and regulatory/ ethics dossiers; conducting monitoring activities; attending investigator meetings; defining recruitment plans; selection clinical sites; overseeing clinical research; evaluating study risks and managing study quality.I have strong experience in leadership positions, participating in process management and team development.I really enjoy executing challenge activities and thinking critically about strategies that should be applied in each project. I am committed to performing high-quality work within the expected deadline and building good connections with internal and external partners. As a result, I developed great communication and writing skills.I am passionate about teaching. Therefore, I dedicate my time to the academic field by teaching classes on clinical trial management and design and keeping up with my studies.