Lucia Farima

Background

About Lucia Farima

Life sciences professional with an advanced understanding of the drug development lifecycle and the overall clinical research process. Experienced in managing end-to-end clinical trial operations, including data management services, across Phase I-IV and non-interventional studies in diabetes, obesity, and oncology therapeutic areas. Successfully delivered single- and multi-service projects with minimal guidance, ensuring quality deliverables on time, within budget, and to customer satisfaction as an FSP resource. Possesses a strong digital affinity and expertise in clinical data management systems, including clinical protocol interpretation, CRF development, and integration of external data sources such as labs and ePRO. Skilled in data cleaning, QC, query resolution supporting clinical decision-making and ensuring compliance with GCP-ICH, regulatory standards (FDA, EMA), CDISC, GCDMP, and data privacy. Highly motivated to do the right thing, committed to data integrity and transparency, and a dedicated problem-solver with a deep passion for clinical data management.