Average Salary for Jobs with FDA Adverse Event Reporting (AE) Skills

The average salary for jobs that require the skills of FDA Adverse Event Reporting (AE) is $137,384 based on United States National Average.

Base Salary

Core compensation

$51,601
$223,168
$137,384
Drug Safety Assessment Director
Alternate Job Titles: Drug Safety Monitoring and Information Director | Drug Safety/Medical Information Director

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


Drug Safety Assessment Manager
Alternate Job Titles: Drug Safety Monitoring and Information Manager | Drug Safety/Medical Information Manager

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


Drug Safety Assessment Manager, Sr.
Alternate Job Titles: Drug Safety Monitoring and Information Manager, Sr. | Drug Safety/Medical Information Manager, Sr.

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


Drug Safety Assessment Specialist I
Alternate Job Titles: Drug Safety Monitoring and Information Specialist I | Drug Safety/Medical Information Specialist I | Entry Drug Safety/Medical Information Specialist

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


Drug Safety Assessment Specialist II
Alternate Job Titles: Drug Safety Monitoring and Information Specialist II | Drug Safety/Medical Information Specialist II | Intermediate Drug Safety/Medical Information Specialist

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