Job Overview
Job Title: Pharmacovigilance Associate (Post Marketing)
Company: ICON plc
Location: São Paulo, Brazil (Homeworking / Remote)
Employment Type: Full-Time
Start Date: 19 May 2026
Closing Date: 18 June 2026
Salary: Competitive
About the Company
ICON plc is a global healthcare intelligence and clinical research organization focused on improving patient safety and advancing clinical development through high-quality research and regulatory compliance.
The company is known for:
Strong pharmacovigilance and drug safety operations
Global clinical research expertise
Inclusive and collaborative work culture
Commitment to regulatory excellence
Role Summary
The Pharmacovigilance Associate will support post-marketing drug safety activities by collecting, analyzing, and reporting adverse event data to ensure compliance with global regulatory standards and protect patient safety.
The role focuses on:
Adverse event management
Signal detection and risk assessment
Regulatory reporting support
Cross-functional collaboration
Pharmacovigilance system maintenance
Key Responsibilities
1. Adverse Event Management
Collect and review adverse event (AE) reports
Ensure accurate and timely reporting in line with regulatory guidelines
Maintain compliance with internal safety procedures
2. Signal Detection & Risk Assessment
Identify potential safety signals
Perform risk evaluation based on safety data
Support safety issue investigations
3. Regulatory Support
Assist in preparation of safety reports
Support regulatory submissions
Ensure adherence to pharmacovigilance regulations and standards
4. Cross-Functional Collaboration
Work with clinical and medical teams
Support safety-related queries and investigations
Communicate findings to relevant stakeholders
5. Compliance & Knowledge Maintenance
Stay updated with pharmacovigilance regulations
Follow industry best practices
Ensure consistent quality and accuracy in reporting
Required Qualifications
Education
Bachelor’s degree in:
Life Sciences
Pharmacy
Related field
Advanced degree preferred
Required Experience
Experience in pharmacovigilance, drug safety, or related clinical/pharmaceutical roles
Exposure to regulatory or clinical safety environments preferred
Required Skills
Strong analytical and data interpretation skills
Attention to detail in reporting and documentation
Excellent communication and teamwork abilities
Knowledge of pharmacovigilance processes
Ability to maintain compliance and quality standards
Strong organizational skills
Key Competencies
Patient safety focus
Regulatory awareness
Data accuracy and integrity
Collaboration across teams
Ability to manage multiple tasks efficiently
Benefits
ICON plc provides:
Health insurance options
Paid annual leave
Retirement and financial planning benefits
Life assurance coverage
Employee Assistance Programme (LifeWorks)
Flexible country-specific benefits (gym, travel, childcare, etc.)
Work-life balance support programs
Work Culture & Inclusion
The company promotes:
Equal opportunity employment
Diversity and inclusion
Safe and respectful workplace environment
Accessibility support for candidates with disabilities
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Mexico |northeastern :
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Saarbrucken |Switzerland :
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Budapest |BULGARIA :
Bulgaria | Vedant |Denmark :
Copenhagen | Denmark |Europe :
Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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Sheffield |Oxfordshire :
Witney |Ontario :
North York | Richmond Hill | Australia | Mississauga | Renfrew | Uxbridge |Canada :
Canada |Quebec :
Montreal |Brussels :
Brussels |Antwerp :
Heist op den Berg |Flemish Brabant :
Zaventem |South America :
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Brazil | Sao paulo |Attica :
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Manila |Croatia :
Croatia |Zagreb :
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Jakarta |East Java :
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Japan | Saitama |Tokyo :
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Oulu |Southwest Finland (Varsinais-Suomi) :
Turku |Remote Korea :
Remote Korea |Republic of Korea :
Seoul |Kazakhstan :
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