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

Try These Other Programs

Pharmacovigilance Programs At Universities | DIA Training