Pharmacovigilance Associate

2 days ago

Remote, India Clariwell Global Full time

Collect and process adverse event (AE) reports from healthcare professionals, patients, and regulatory authorities.
- Perform case intake and data entry into safety databases (e.g., Argus, ArisG).
- Assist in triaging and prioritizing cases based on seriousness and timelines.
- Perform quality checks to ensure accuracy and completeness of information.
- Draft case narratives and perform medical coding (MedDRA).
- Support Periodic Safety Update Reports (PSURs), Risk Management Plans (RMPs), and other regulatory documents.

Work Location: Remote

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