Beatriz Rabago

Background

About Beatriz Rabago

Highly experienced professional, with 19-years background in Clinical Research, managing the execution of multinational clinical trials (phases II, IV and third-party unblinded studies), from site selection through to close-out, across multiple therapeutic areas. Experienced in: Project Management of highly complex large-sized clinical trials, cross-functional project teams coordination, management of internal audits and inspections, leader of ads campaigns to enhance patients' recruitment, responsible for contracts drafting, design of study tools and documents, reviewer of monitoring visit reports, Quality Control Visits and Co-Monitoring Visits to hospitals, CROs oversight, involvement in protocol feasibilities and sites selection; assistance in the identification of quality issues and in the implementation of corrective actions; selection, training and coaching of new staff; accountable for all submissions and communications to the relevant regulatory authorities; primary liaison with other functional teams within the company to manage study requirements; vendors selection and oversight; contracts and budgets negotiation, invoicing, financial expertise. European Project Manager Representative within international study teams, speaker at international investigators' meetings to present protocol study procedures. Specialties: CNS (Neurology), Transplantation (renal, liver and heart), Trauma, Pediatrics, Vaccines, Oncology, Dermatology, Respiratory, Woman’s Health. Good Clinical Practices.