Associate I, Pharmacovigilance & Safety Reporting

Fortrea, located in Mexico City, seeks a detail-oriented professional for managing adverse event reports in clinical research. Responsibilities include data entry, quality review, and regulatory compliance for safety reports. The ideal candidate will have expertise in pharmacovigilance, strong analytical skills, and a commitment to excellence in safety management.
Fortrea values diversity and is an equal opportunity employer. We encourage applications from all qualified individuals regardless of their background.
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