Remote Pharmacovigilance Regulatory Reporting Specialist

IQVIA

Buenos Aires

Remote

ARS 600,000 - 900,000

Full time

14 days+

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Job summary

IQVIA is seeking a Regulatory Reporting Specialist to support safety report submissions to regulatory authorities. This 100% home-based role reviews, processes, and distributes safety data to internal teams and external parties in line with SOPs and regulations.

It is a tri-lingual position requiring fluency in English, Spanish, and Portuguese. Required: life sciences degree; 1 year in pharmacovigilance (regulatory reporting preferred); knowledge of Argus and medical terminology; strong

Qualifications

Bachelor's degree in life sciences.
Languages: Advanced level of English, Spanish and Portuguese.
1 year of experience in pharmacovigilance activities (mandatory).
Experience with Argus desirable.
Good knowledge of medical terminology and safety databases.
Strong organizational skills and ability to work independently and in a team.

Responsibilities

Process safety data according to applicable regulations, guidelines, SOPs, and project requirements.
Review, assess, and process safety information from various sources and distribute reports to internal and external parties.
Ensure compliance with quality, productivity, and delivery standards per project requirements.
Track cases and liaise with health care professionals to address project-related issues.
Attend project team meetings and provide feedback to the operations manager on challenges, issues, or successes.