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Regulatory Affairs Manager
- IQVIA
- Madrid, Spain, Spain
- Level:Manager
- Posted
Source: IQVIA’s own career site First seen
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Job Overview. Individual contributor with advanced knowledge acquired from at least 8 years of relevant industry experience. Working independently with limited supervision, the individual will provide strategic regulatory expertise and leadership for clinical trial applications and lifecycle management activities, with a strong focus on EU Clinical Trials Regulation (CTR) submissions and Clinical…
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