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Adverse Event Report Specialist
hace 2 semanas
The Adverse Event Report Specialist is responsible for the timely and accurate processing of adverse event reports. This position involves receiving, reviewing, and processing incoming reports from various sources, including healthcare professionals and regulatory agencies.
Responsibilities:- Receive and review incoming reports
- Triaging reports based on severity and urgency
- Accurately entering data into safety databases
- Conducting initial case assessments and assigning case status
This specialist will also be responsible for tracking and monitoring the progress of AE investigations and collaborating with internal stakeholders to ensure compliance with relevant regulations.
Requirements:- Bachelor's degree in life science or equivalent experience
- Excellent written and verbal communication skills
- 1 year of experience in pharmacovigilance or related field preferred
- Strong problem-solving and analytical skills
