Maintain safety reporting requirements for expedited and periodic reports, line listings, for Regulatory Authorities, Ethics Committees, and investigators within specified timelines as well as other Pharmacovigilance intelligence as per assignment and in accordance with company procedures.

• Maintain a strong understanding of ICON's Pharmacovigilance intelligence systems, processes, and conventions

• Maintain a strong understanding of ICON Standard Operating Procedures (SOPs), Working Procedures (WPs), guidance documents and manuals associated with Pharmacovigilance intelligence.

• Perform oversight of assigned projects ensuring all ICON, Sponsor, and regulatory timeframes are met for the maintenance of related global safety reporting intelligence requirements.

• Operate in a lead capacity ensuring ownership and accountability of safety reporting intelligence on assigned projects.

• Ensure completion of all assigned project activities accurately and in accordance with ICON standards, regulatory requirements, and client contractual obligations.

Collaborate with various parties such as project team members and client contacts as applicable. Build and maintain good relationships across functional units.

• Work within multiple databases. Maintenance of Pharmacovigilance intelligence information with timely updates to the intelligence databases.

 Travel (approximately 10%) domestic and/or international, as required.

What you need:

• Bachelor's degree in life sciences

• Circa 4 years of experience in a similar position in pharmacovigilance

• Fluency in English language

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

• In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.