Coordinador(A) De Admisiones | Liderazgo En Captación

Instituto-Universitario-Del-Centro-De-M; Benito Juárez; À distance; MXN 300 000 - 420 000; Plein temps

Avantages offerts par ce poste

Remote-first environment

Fully remote role

Résumé du poste

Instituto-Universitario-Del-Centro-De-M is seeking a Coordinador de Farmacovigilancia for a fully remote role. You will help safeguard patient safety by monitoring adverse events from home, across regions.

You will receive, assess, and process reports, ensure data integrity in the pharmacovigilance database, and support global regulatory compliance with internal teams and external partners.

Qualifications

• Experience in pharmacovigilance or clinical safety.
• Strong attention to detail and data entry accuracy.
• Ability to work remotely and coordinate with global teams.

Responsabilités

• Receive, assess, and process adverse event reports.
• Ensure accurate data entry into pharmacovigilance systems.
• Maintain compliance with global and local regulations and guidelines.

Connaissances

Pharmacovigilance

Regulatory compliance

Data entry accuracy

Remote collaboration

Outils

Pharmacovigilance database

Description du poste

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