Global Patient Safety Evaluation Post-Doctoral Fellowship Program
Global Patient Safety Evaluation (2 years)
With a mission to ensure patient safety, the Global Patient Safety Evaluation (GPSE) function at Takeda is responsible for pharmacovigilance (PV) activities including the detection, assessment, management, monitoring, prevention of adverse events and continuous assessment of the benefit-risk profile for all Takeda products. Excellence in Patient Safety requires mastery of medical and scientific disciplines as well as operational excellence and compliance. The purpose of Takeda’s two-year fellowship program is to provide the fellow with in-depth training in safety risk assessment, characterization, and minimization/mitigation. Fellows work closely with experts in Pharmacovigilance, specifically with PV Scientists and Global Safety Leads, as well as with other GPSE colleagues and cross-functional groups. Fellows are dedicated to PV activities for both investigational and marketed products during the course of the fellowship and have the opportunity to rotate across therapeutic areas.
Location: Cambridge, MA
Global Patient Safety Evaluation Current Fellows
Additional Resources:
Overview of Pharmacovigilance from the EMA (European Medicines Agency)
Jobs for you
- Medical Director, Clinical Science, NS TAU- Respiratory/Sleep Disorder Cambridge, Massachusetts Category: Clinical Development
- Medical Director, Clinical Science, NS TAU- Stroke Neurologist Cambridge, Massachusetts Category: Clinical Development
- Associate Director, Process Design & Improvement Boston, Massachusetts Category: Project/Process Management
- Preclinical Research Scientist for Neuroscience Drug Discovery Fujisawa, Japan Category: Research Science
You have not viewed any jobs yet.
You have not saved any jobs yet.
