Laura Oliva Pérez

Clinical research professional with 8 years of experience supporting global Phase I–IV clinical trials within hospital and sponsor-facing environments. Strong background in clinical trial monitoring and coordination, TMF management, study start-up to close-out activities, site oversight, and cross-functional collaboration. Proven ability to ensure compliance with GCP, ICH, SOPs, and regulatory requirements. 

Currently based in Spain, with a long-term plan to relocate to Doha for family reasons, as my partner has moved there for work. Motivated by international environments and long-term professional growth within global clinical research settings.

Currently working as a Clinical Research Associate at Dexeus, in charge of data monitoring, TMF management, quality audits and regulatory activities. 5 years of experience as a Clinical Trial Coordinator in Oncology and 2 years as a Clinical Trial Coordinator with medical devices.

Master’s degree in Clinical Research and Translational Oncology, with a Bachelor’s degree in Molecular Biology. Complemented by specialized training in Regulatory Affairs (FDA/EMA), Quality in the Pharmaceutical Industry, Advanced Excel, and data-related tools. Continuous learner with a strong interest in data analysis and process optimization.