FE

Freelance Lead/Srcra Spain Regulatory Consultant - Ctis Expert

Freelance Global Study Start Up Associate at Advanced Clinical

Freelance Lead/SrCRA Spain Regulatory Consultant and CTIS expert has extensive experience in clinical research and regulatory affairs, serving in various roles since 2012. As a Freelance Global Study Start Up Associate at Advanced Clinical, responsibilities include coordinating regulatory processes in Spain, with a focus on Ethics Committee and Competent Authority submissions. Previous roles encompass Clinical Operations Manager at PMC PARTNERS RESEARCH SL, Freelance SrCRA positions at HOYA Surgical Optics and PSR Orphan Experts, and significant involvement in a COVID-19 vaccine phase 3 trial while working with IQVIA. Educational qualifications include a Master's Degree in Clinical Biology from Universidad Complutense de Madrid and a Master's Degree in Clinical Trial Monitoring from Universidad Autónoma de Madrid, along with certifications in Clinical Project Management and strategic direction.

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