I am a pharmacist with over 15 years of experience in the pharmaceutical industry, primarily in medical information and regulatory-related roles. Throughout my career at Pfizer and MSD, I have worked in highly regulated environments supporting global and regional product portfolios across North America, Latin America, and the Caribbean. My work has focused on translating complex scientific and regulatory information into clear, evidence-based communications that support healthcare professionals, internal stakeholders, and cross-functional teams.
Some of my key achievements include leading medical information strategies for multiple therapeutic areas, managing scientific content used across several markets, and collaborating with global product teams to ensure consistent and compliant communication of scientific data. I have also supported regulatory processes, medical review committees, and cross-functional initiatives involving regulatory, safety, legal, and commercial teams.
Overall, my experience has allowed me to develop strong capabilities in scientific communication, regulatory environments, stakeholder collaboration, and working within complex global organizations.More...