Pharmacovigilance Associate

Job Description:

• 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.