About this role
About the Role Pharmacovigilance Associate at ICON plc will monitor and ensure the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information. You will deliver pharmacovigilance and drug safety work to a high standard, working closely with your team and stakeholders. What You'll Do
- Collecting and reviewing adverse event reports to ensure accurate and timely reporting in accordance with regulatory guidelines.
- Conducting signal detection and risk assessment activities to identify potential safety issues.
- Collaborating with cross-functional teams to support safety-related inquiries and investigations.
- Maintaining up-to-date knowledge of pharmacovigilance regulations and industry best practices.
- Assisting in the preparation of safety reports and regulatory submissions. What We're Looking For
- 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 environment.
- 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.
- A commitment to maintaining high standards of quality and compliance in all pharmacovigilance activities.
- Willingness to travel as required (approximately 10%). Compensation & Benefits
- Our benefits include a diverse range of annual leave entitlements, health insurance offerings, competitive retirement planning, and a Global Employee Assistance Programme (LifeWorks) with 24-hour access to a global network of professionals for well-being support.
- Life assurance and flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, and health assessments.
- ICON is committed to inclusion and providing an accessible environment for all candidates.