PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries.
Post : Drug Safety Specialist
Requirement of a candidate with minimum of 5-6 years of relevant xEVMPD and IDMP experience.
• Experience in IDMP data collection, data transformation and execution of test case scenarios for EMA.
• Experience in XEVMPD management and submission to Health Authority
• Knowledge of the PLM (Product Lifecycle Management) portal
• Preparing documents for changes and updating User Acceptance Test (UAT) and Product Specification Document (PSD)
Experience : minimum of 5-6 years
Location : Mohali
Job ID : R0000014870
Industry Type : Pharma/ Healthcare/ Clinical research
Last Date : 15th September, 2023