Senior PV Lead: Adverse Event Data & Safety Submissions

A clinical research organization seeks a Senior Associate, Pharmacovigilance to oversee the collection, processing, and reporting of Serious Adverse Event data. Responsibilities include authoring Safety Management Plans, reviewing SAE data, and generating regulatory reports. Candidates should have a Bachelor's degree in a science-related field or nursing and at least 5 years of pharmacovigilance experience. Strong skills in communication, organization, and database management are essential for success in this role based in Mexico.
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