Coordinador De Seguridad Patrimonial

Ferretera Sa De Cv; Tlalnepantla; Remote; MXN 260,000 - 420,000; Full time

Job summary

Ferretera Sa De Cv is seeking a detail-oriented Pharmacovigilance Coordinator to join a fully remote team. The role focuses on ongoing safety monitoring of pharmaceutical products by managing adverse event reports from multiple sources.

You will collaborate with internal departments and partners to ensure regulatory compliance and robust pharmacovigilance systems on a global scale, contributing to patient safety and data integrity in a distributed work environment.

Qualifications

• Background in pharmacovigilance and patient safety.
• Experience with adverse event processing.

Responsibilities

• Receive, assess, and process adverse event reports from various sources.
• Ensure accurate and timely data entry into the pharmacovigilance database.
• Maintain compliance with global and local pharmacovigilance regulations and guidelines.
• Support the preparation of periodic safety reports.

Skills

Pharmacovigilance

Data entry

Regulatory compliance

Education

Pharmacy degree

Job description

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Ayer

About the Role

Our client, a global leader in pharmaceutical innovation, is seeking a detail-oriented and proactive Coordinador de Farmacovigilancia to join their team. This is a fully remote position, allowing you to contribute to patient safety from the comfort of your home. Your primary responsibility will be to ensure the ongoing safety monitoring of our pharmaceutical products by managing and processing adverse event reports. You will collaborate closely with internal departments and external partners to maintain robust pharmacovigilance systems and ensure compliance with regulatory requirements worldwide. The ideal candidate has a strong background in pharmacy or a related healthcare field, a thorough understanding of pharmacovigilance principles, and exceptional organizational skills. We are committed to a remote-first work environment, providing comprehensive support and resources to our distributed team members. This role offers a significant opportunity to impact public health by safeguarding the safety profile of vital medications. Your dedication to accuracy and regulatory adherence will be critical in maintaining trust and ensuring the well-being of patients who rely on our treatments.

Key Responsibilities

• Receive, assess, and process adverse event reports from various sources.
• Ensure accurate and timely data entry into the pharmacovigilance database.
• Maintain compliance with global and local pharmacovigilance regulations and guidelines.
• Support the preparation of periodic safety