Pharmacovigilance Specialist
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Job Description
Pharmacovigilance Specialist analyzing adverse events and preparing regulatory safety reports for ICON’s global clinical research organization.
Responsibilities:
- Monitor the safety of pharmaceutical products by analyzing, interpreting, and reporting adverse event data in accordance with regulatory requirements
- Take responsibility for pharmacovigilance and drug safety deliverables, ensuring quality and efficiency
- Collect, review, and analyze adverse event reports for timely and accurate regulatory reporting
- Conduct risk assessments and signal detection activities to identify and evaluate potential safety concerns
- Collaborate with cross-functional teams on safety-related inquiries and investigations
- Prepare and submit safety reports and regulatory submissions
- Stay current on pharmacovigilance regulations and industry best practices
Requirements:
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Experience in pharmacovigilance, drug safety, or a related area, preferably within a clinical or pharmaceutical setting
- Strong analytical skills and attention to detail in data collection and reporting
- Excellent communication and interpersonal skills, enabling effective collaboration with diverse teams
- A commitment to upholding high standards of quality and compliance in all pharmacovigilance activities
- Willingness to travel as required (approximately 15%)
- 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
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