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Adverse event reporting specialist

Embu das Artes
beBeePharmacovigilance
Eventos
Anunciada dia 4 outubro
Descrição

Role Overview

We are seeking a strategic liaison between business users, regulatory teams, and IT to ensure pharmacovigilance systems and workflows enable accurate, compliant, and efficient adverse event reporting.

This role combines strong product ownership responsibilities with deep domain expertise in pharmacovigilance, regulatory compliance, and technology. The analyst will oversee end-to-end product roadmaps, ensuring alignment with business needs, and drive platform upgrades, integrations, and compliance.

Key Responsibilities:

* Product Ownership & Roadmap
* Own and manage the PV product roadmap, ensuring alignment with business priorities.
* Oversee platform maintenance, rebuilding, and tech stack upgrades (e.g., cloud migration).
* Stay updated on latest pharmacovigilance and product technology trends.
* Cross-Functional Collaboration
* Work closely with Business, Infrastructure, and Leadership teams to plan/manage product releases, downtime, incidents, and upgrades.
* Serve as the key liaison across regulatory, clinical operations, QA, and IT functions.
* System Integration & Compliance
* Oversee safety system integrations (Argus, ArisG, Veeva Vault Safety) ensuring accurate data flow and reporting.
* Ensure Argus acts as the central system, receiving case data from call centers, flowing through safety systems, and reaching regulatory authorities with compliance documentation.
* Support signal detection and reporting in line with global compliance and regulatory standards.
* Monitoring, Debugging & Quality
* Perform monitoring and debugging for system issues such as unprocessed cases, reconciliation gaps, and data discrepancies.
* Review AWS logs and system access for issue resolution.
* Collaborate with QA for system quality checks, validation, and signal monitoring.
* Analysis & Documentation
* Gather and analyze requirements for PV systems and workflows.
* Document processes, data flows, and system functionalities related to adverse event reporting.
* Support validation and user acceptance testing (UAT).
* Provide user training, support, and knowledge sharing.

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