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Adverse Event Processor
hace 2 semanas
About the Role
\We are seeking an experienced Case Intake Specialist to join our Pharmacovigilance team. The successful candidate will be responsible for receiving, processing, and tracking adverse event reports to ensure compliance with regulatory requirements.
\The Key Responsibilities of this role include:
\Intake and processing of adverse event reports, including data entry and maintenance of accurate records.
Conducting initial assessment and triage of adverse events to determine seriousness and reportability.
Collaboration with internal stakeholders and external partners to ensure efficient case processing and data management.
Requirements
\To be successful in this position, you should have:
\A strong background in pharmacovigilance or a related field (e.g., clinical research, medical information).
Excellent written and verbal communication skills, with fluency in English and local languages.
Ability to work independently and as part of a team.
About IQVIA Argentina
\IQVIA Argentina is dedicated to ensuring the safety of our products through adherence to regulatory guidelines and internal Standard Operating Procedures (SOPs).
