Safety Science Coordinator

Role & Responsibilities

• Process Expedited Safety Reports (ESRs) and Periodic Safety Reports (PSRs).
• Log and track Adverse Events (AE) and Serious Adverse Events (SAE).
• Write patient narratives and code events using MedDRA.
• Support safety report submissions and maintain safety databases.
• Assist in quality review, reconciliation, and audit readiness.
• Train and mentor junior staff.

Qualifications & Experience

• PharmD, MS/MA in Life Sciences, or BS/BA in related fields.
• 1-2 years of experience in safety, pharmacovigilance, or clinical research.

Skills

• Knowledge of AE/SAE processing and safety databases.
• Strong attention to detail and data accuracy.
• Proficiency in MS Office and Windows.

About the Company
Fortrea is a global leader in clinical research and pharmacovigilance, providing safety and regulatory services to biopharmaceutical companies worldwide.