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Director, Medical Safety- Sponsor-Dedicated (Home-based)
- IQVIA
- Zagreb, Croatia, Croatia
- Level:Director / Head of
- Posted
Source: IQVIA’s own career site First seen
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Responsibilities. - Conduct medical review of clinical trial and post-marketing safety data, including adverse events (AEs), adverse drug reactions (ADRs), coding, causality, expectedness, seriousness assessments, and benefit-risk evaluations.
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