What is a Clinical Trials Pharmacovigilance Specialist
Monitors and reports adverse events, manages safety databases, and ensures compliance with pharmacovigilance regulations for clinical trials and marketed products.
Clinical Trials Pharmacovigilance Specialist Core Duties
Collect And Evaluate Adverse Event Reports | Manage Safety Databases And Aggregate Safety Reports | Ensure Timely Regulatory Reporting | Support Signal Detection And Risk Management | Liaise With Safety Committees.
Clinical Trials Pharmacovigilance Specialist Education Requirements
Bachelor Or Master Degree In Pharmacy Or Life Sciences With Pharmacovigilance Training
Clinical Trials Pharmacovigilance Specialist License and Accreditation Agency
PV Credential | Employer Credential
Clinical Trials Pharmacovigilance Specialist Program Length
6 to 36 Months
Clinical Trials Pharmacovigilance Specialist Salary Min and Max
$60000 to $140000
Clinical Trials Pharmacovigilance Specialist Work Settings
Pharma Companies | CROs | Regulatory Agencies | Academic Research Centers
Clinical Trials Pharmacovigilance Specialist Key Skills
Adverse Event Reporting | Safety Database Management | Regulatory Reporting | Signal Detection
Look for These Programs
Pharmacovigilance Programs At Universities | DIA Training