Pharmacovigilance Associate

• Collects adverse event data on all marketed products and those in development.
• Implements and manages adverse event processes and databases.
• Ensures regulatory compliance for both expedited and periodic reports.
• Provides integrated strategic safety expertise to clinical developrams.
• Performs active pharmacovigilance with rapid identification and analysis of safety signals, to define emerging drug safety profiles of all products and drive patient risk management.
• Delivers high-quality product safety data and analysis to internal and external customers throughout the product life cycle
• Contributes to process improvements
• Typically resolves problems using existing solutions
• Provides informal guidance to junior staff - Works with minimal guidance
• Requires in-depth knowledge and experience
• Solves complex problems; takes a new perspective using existing solutions
• Works independently; receives minimal guidance
• Acts as a resource for colleagues with less experience
• Represents the level at which career may stabilize for many years or even until retirement Undergraduate/BA/BS degree in applicable discipline and 3-5 Yrs of related experience.

Regards,

Indu

Clinical Recruiter

732-844-8725

indu @irionline.com