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Pharmacovigilance Regulatory Reporting Specialist

São Paulo, Brazil🌐 Remote💼 Full-time🗓 2026-07-12 → 2026-07-30

Core

Submit safety reports to regulatory authorities and process safety data from various sources.

Role type

Pharmacovigilance Regulatory Reporting Specialist

Builds

Safety reports for regulatory authorities

Domain

Life sciences / Pharmacovigilance

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

Regulatory reporting, Argus, medical terminology, safety databases

Preferred skills

None stated

Technologies

Argus

Responsibilities

Process safety data according to regulations and SOPs, ensure compliance with quality and delivery standards, track cases per project plan, report quality problems to senior team members, liaise with functional team members and healthcare professionals, attend project team meetings and provide feedback to operations manager

Seniority

Mid-level, hands-on IC

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