The average salary for jobs that require the skills of FDA Adverse Event Reporting (AE) is $137,384 based on United States National Average.
Core compensation
Directs enterprise drug safety assessment and pharmacovigilance programs to ensure compliance with global safety regulations and support organizational risk management objectives. Oversees safety surveillance, signal detection, aggregate reporting, risk evaluation, and governance activities for marketed and investigational products. Develops pharmacovigilance strategies, policies, and operational ... View job details
Manages drug safety assessment programs and pharmacovigilance operations to ensure effective monitoring, evaluation, and reporting of product safety information across the organization. Directs adverse event processing, case review, aggregate reporting, and safety surveillance activities in compliance with global regulatory requirements and company policies. Develops and implements pharmacovigilan... View job details
Manages drug safety assessment programs and pharmacovigilance operations to ensure effective monitoring, evaluation, and reporting of product safety information across the organization. Directs adverse event processing, case review, aggregate reporting, and safety surveillance activities in compliance with global regulatory requirements and company policies. Develops and implements pharmacovigilan... View job details
Supports drug safety assessment and medical information activities by evaluating adverse event reports, responding to medical inquiries, and ensuring compliance with pharmacovigilance regulations and company standards. Reviews, documents, and processes adverse event and product quality complaint reports to identify new, unknown, or changing risks associated with a drug or medicine. Evaluates drug ... View job details
Supports drug safety assessment and medical information activities by evaluating adverse event reports, responding to medical inquiries, and ensuring compliance with pharmacovigilance regulations and company standards. Reviews, documents, and processes adverse event and product quality complaint reports to identify new, unknown, or changing risks associated with a drug or medicine. Evaluates drug ... View job details
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