Regulatory Affairs Specialist, IQVIA Biotech
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Description
We are looking for a Regulatory Affairs professional to join our IQVIA Biotech Regulatory Affairs team, supporting clinical research projects across Europe.
In this role, you will provide regulatory expertise and hands-on support throughout clinical development, with a particular focus on EU Clinical Trials Regulation (EU CTR) submissions.
You will work as part of a global, project-based team supporting primarily drug development programs, including chemical entities and biologics.
This is a gr…
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