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Associate Director Quality Assurance Pharmacovigilance Clinical Audits

Jobleads-US
Princeton, NJ Full Time
POSTED ON 4/10/2025
AVAILABLE BEFORE 5/8/2025

Key Responsibilities

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  • Conduct Pharmacovigilance and Clinical audits for studies and postmarketed products per EMA, FDA, and MHRA regulations and guidelines.
  • Plan, execute, and complete Pharmacovigilance audit program based on risk assessment for all marketed products, clinical trials, vendors, and critical computerized systems.
  • Audit activities include all aspects of planning, conducting, reporting, observations follow-up, and procedural documentation associated with internal and external audits.

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