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Medical Content Specialist
Pharmacovigilance specialist at Novartis who submitted 2,000+ safety cases yearly with 99% on-time compliance and zero critical findings.
ArgentinaMedical Content Specialist at GSK S.A.
Led end-to-end medical review processes, approving 200 scientific materials per month while ensuring accuracy and compliance with local regulatory requirements. Reviewed promotional and non-promotional materials across LATAM markets.
Medical Content ReviewRegulatory CompliancePromotional MaterialsScientific WritingVeeva Promomats
Managed pharmacovigilance case management, submitting over 2,000 safety cases per year to health authorities with 99% on-time compliance and zero critical findings. Led safety signal detection and trained teams on GDP and safety data management systems.
ICSR ManagementSUSARsANMATPharmacovigilanceSignal DetectionMedDRAICH GCPSDVCAPAGDPPower AutomateAI Agents
Oversaw pharmacovigilance operations, managing over 300 safety case reports per year and supporting regulatory submissions. Prepared and distributed safety reports and executed medical information deliverables.
PharmacovigilanceSafety CasesSUSARsPBRERsMedical InformationJasperAdverse Event Triage
Assisted in experimental studies and clinical research projects, applying scientific evidence in decision-making and disseminating scientific information to specialized audiences.
Clinical ResearchScientific EvidenceResearch Protocols
Completed residency in gynecology and reproductive medicine, providing clinical care and gaining specialized medical training.
GynecologyReproductive MedicineClinical Care
Provided general medical care in a clinical practice setting.
General MedicineClinical Practice
Advised on regulatory matters within the disease control service of the government health department.
Regulatory AffairsPublic Health
Completed a medical assistance internship in the emergency room, gaining hands-on clinical experience.
Emergency MedicineMedical Assistance
Clinical Research Monitor certification in progress, expected completion in 2026.
Clinical Research Monitor certification in progress, expected completion in 2026.
AI Automation certification completed in August 2026.
AI Automation certification completed in August 2026.
Specialization in Gynecology and Human Reproduction.
Magister Scientiarum in Biology of Human Reproduction.
Medical Doctor degree.
Power BI and AI use in data analysis certification completed in May 2026.
Power BI and AI use in data analysis certification completed in May 2026.
Certification of Good Clinical Trial Practices: Specialization in ICH Guidelines.
Clinical Research Certification in Design and Interpretation of Clinical Trials.