A global clinical research organization is seeking a Senior Associate in Pharmacovigilance in Mexico to lead the collection and reporting of adverse event data. The ideal candidate will have a Bachelor's degree in a science-related field, at least 5 years of pharmacovigilance experience, and excellent communication skills. Responsibilities include generating regulatory reports and ensuring data accuracy. A positive attitude and the ability to manage multiple priorities are essential for success in this role. The position may require limited travel.