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Regulatory and Start Up Admin - Poland
- IQVIA
- Warsaw, Poland, Poland
- Posted
Source: IQVIA’s own career site First seen
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Job Overview. Perform tasks in support of the Clinical Trial Submission Coordinator (CTSC), Regulatory CTA SM and GCO country teams to make all clinical trial initial submissions, clinical trial amendment submissions and clinical trial notifications in CTIS and track the progress of submissions/notifications. Essential Functions.
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