Pharmacovigilance Associate
Posted 5hrs ago
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Job Description
Pharmacovigilance Associate reviewing adverse events and supporting drug safety reporting at ICON, a global healthcare intelligence and clinical research organization. Conducting signal detection and regulatory submissions.
Responsibilities:
- Monitor and ensure the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information
- Deliver pharmacovigilance and drug safety work to a high standard
- Collect and review adverse event reports for accurate and timely reporting in accordance with regulatory guidelines
- Conduct signal detection and risk assessment activities to identify potential safety issues
- Collaborate with cross-functional teams on safety-related inquiries and investigations
- Maintain up-to-date knowledge of pharmacovigilance regulations and industry best practices
- Assist in preparing safety reports and regulatory submissions
Requirements:
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Experience in pharmacovigilance / drug safety within a clinical or pharmaceutical environment
- Ability to review and process safety events
- Strong analytical skills with attention to detail in data collection and reporting
- Excellent communication and interpersonal skills, enabling effective collaboration with team members and stakeholders
- Commitment to maintaining high standards of quality and compliance in all pharmacovigilance activities
- Willingness to travel as required (approximately 10%)
- Legal right to work in the country where the role is based
Benefits:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways














