Pharmacovigilance

Preferred knowledge of other related disciplines e.g. clinical, regulatory affairs, clinical statistics relevant to aggregate report writing and clinical development 

Serve as the accountable business system owner for PV-related platforms, including safety databases, signal management tools, medical information systems, literature monitoring solutions, and reporting platforms

Basic knowledge of medical terminologies and able to understand common medical terms relevant to pharmacovigilance and adverse event reporting.

Pharmacovigilance Scientist, Senior Scientist ensures regulatory compliance and safety of Takeda's products by managing large projects, developing innovative solutions, and leading teams. This role contributes to the development and execution of pharmacovigilance strategies, ensuring patient safety and regulatory adherence

Act as team lead, owning end-to-end case quality from coding through causality to final company comment. Perform and oversee medical review of ICSRs within defined time standards, ensuring accuracy in Argus.

A Bachelors degree in life sciences or a related field, combined with 5–10 years relevant pharmacovigilance experience. 

Your day to day interactions are with peers within Accenture. You are likely to have some interaction with clients and/or Accenture management. Accenture

Pharmacovigilance (PV) Associate will be responsible for all assigned Clinical Safety and post-marketing PV activities. The PV Associate will be part of the newly developed, lean and efficient, Global Safety Data Management team