silviaoli1983

About: Profile Summary: Research Professional with solid background in biological sciences and over 10 years of hands-on experience in clinical site monitoring, local project coordination, and data quality. Effective collaboration with multidisciplinary and diverse teams across Portugal, Spain, UK, and Holland. Experienced in a wide range of clinical areas including oncology, infectious diseases, rare pediatric conditions. Driven by meaningful research that impact people’s lives, strengthens communities and promotes continuous development. Clinical Research Experience: Experienced in managing and supporting clinical research projects across a broad range of therapeutic areas, including: Invasive Bladder Cancer; SARS-CoV-2 Infection (Paediatric and Pregnancy); Clostridium difficile Infection; Non-small Cell Lung Cancer; Systemic Lupus Erythematosus; Arginase 1 Deficiency (Paediatric); Hemophilia A (Paediatric); Metastatic Hormone-Naive and Castration-Resistant Prostate Cancer; Active Psoriatic Arthritis; Crohn’s Disease; Nonalcoholic Steatohepatitis (NASH); Non-cystic Fibrosis Bronchiectasis with Pseudomonas aeruginosa; HIV Infection; Chronic Hepatitis B and C Virus Infections; Advanced Follicular Lymphoma; Philadelphia Chromosome-Positive Acute Lymphoblastic Leukaemia (Paediatric); Metastatic Breast Cancer; Amyloidosis AA; Complicated Urinary Tract Infections; Primary Progressive Multiple Sclerosis; Type 2 Diabetes; and Acute Coronary Syndrome. Professional Activities: Conducted activities both remotely and on-site to support the effective implementation of new clinical study protocols across diverse healthcare units. Provided technical support to research teams, ensuring participant safety, data quality, and regulatory compliance. Monitored adherence to study protocols, ICH-GCP guidelines, Ethics Committee requirements, EU and national regulations, and Sponsor SOPs and Work Plans. Career Objective: I am currently pursuing new professional opportunities in clinical research with a focus on project development, management, and auditing. I aim to contribute to scientifically rigorous studies that prioritize the perspectives and well-being of participants and communities. I am dedicated to applying effective tools and methodologies for the development and implementation of diverse study protocols that meet the highest quality, ethical, and regulatory standards.