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- Performing Pharmacovigilance activities per project requirement.
- Collecting and tracking incoming Adverse Events and endpoint information.
- Receiving, reviewing, and interpreting medical reports.
- Processing safety data according to applicable regulations, guidelines, Standard Operating Procedures (SOPs), and project requirements.
You will work closely with senior operation team members to distribute reports onwards to both internal and external third parties, following applicable regulations, SOPs, and internal guidelines.
