Job Summary

• As a Senior Pharmacovigilance Associate at ICON, you will play a pivotal role in overseeing the medical aspects of pharmacovigilance activities, ensuring the safety of investigational drugs and contributing to the advancement of innovative treatments and therapies.
• This role is responsible for conducting comprehensive medical review of Individual Case Safety Reports (ICSRs), ensuring the accuracy, integrity, and compliance of global regulatory reports, and for collaborating cross functionally and providing technical leadership within Case Management and across Global Patient Safety (GPS).
• ICON offers a diverse and inclusive culture with competitive salary and benefits focused on well-being and work-life balance, including health insurance, retirement planning, and global employee assistance programs.

Matching Summary

Skills & Requirements

Key Requirements

• BS degree in health-related or scientific field
• 3-5 years clinical experience or 2-5 years pharmaceutical experience
• At least 2 years clinical development experience
• Safety case processing experience required
• Fluent English communication

Work Rights