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This role is crucial in ensuring the integrity and efficiency of adverse event intake processes. As an Adverse Event Intake Coordinator, you will be responsible for receiving, reviewing, and processing incoming adverse event reports from various sources.
Responsibilities:- Process incoming AE reports, conducting thorough reviews and assessments.
- Develop and implement effective systems for tracking and monitoring AE cases.
- Collaborate with cross-functional teams to ensure seamless case processing and resolution.
- Prepare and submit high-quality safety reports to regulatory agencies.
- Bachelor's degree in a life science field or equivalent experience.
- Excellent communication and problem-solving skills.
- Proficiency in Microsoft Office Suite.
- Experience in pharmacovigilance or a related field preferred.