Coordinador Operativo Zona Norte - Cdmx Y Edomex

Grupo IPS; Cuautitlán de García Barragán; A distancia; MXN 360.000 - 480.000; Jornada completa

Descripción de la vacante

Grupo IPS is seeking a detail-oriented Coordinador de Farmacovigilancia to monitor the safety of pharmaceutical products from a remote location. The role centers on managing adverse event reports and ensuring data integrity across a global pharmacovigilance program.

The candidate should possess a strong background in pharmacy or healthcare and a thorough understanding of pharmacovigilance principles, with a focus on regulatory compliance and risk management.

Responsabilidades

• 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

Descripción del empleo

Coordinador de Farmacovigilancia

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