Barbara Scangarelli

 a professional with over 25 years of solid experience in the pharmaceutical industry, the last 12 of which have been dedicated to clinical research coordination. Throughout my career, I have worked on national and international projects, conducting multicenter studies with a focus on regulatory, ethical, and scientific excellence. My skills include developing and reviewing protocols, selecting study sites, training teams, and supervising participant recruitment and monitoring. I have experience in resource management, feasibility, contract management, and resource management, ensuring compliance with budgets and schedules. I maintain continuous communication with investigators, sponsors, and teams for the preparation of reports. Committed to regulatory and ethical compliance, I have worked on more than 99% of regulatory approvals from international audits for vaccine exports and new drug registrations. My focus is to contribute to the innovation, safety, and efficacy of new drugs and vaccines, both nationally and internationally.

My passion for medical innovation and direct contact with healthcare professionals now leads me to a strategic transition to the role of Medical Science Liaison (MSL) — a position where I can combine my technical background with my interpersonal communication skills and robust network of medical contacts.

I have expertise in national and international audits and monitoring, mastery of good clinical practices (ICH-GCP), experience in multicultural environments, and am fluent in Portuguese and English, as well as intermediate Spanish.

I am open to challenges in remote, hybrid, or face-to-face environments, with full availability for travel. My purpose is to contribute to scientific advancement and be a reliable link between science and clinical practice.