Global Lead Medical Writer - Regulatory Submissions
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IQVIA is seeking a Principal Medical Writer to lead the development of regulatory documents for submissions to regulatory authorities worldwide.
You will provide strategic direction to cross-functional project teams to ensure data-driven clinical messages are accurate and well-presented.
The role requires a Bachelor’s degree (advanced degree preferred) and at least 5 years of medical writing experience in the biopharmaceutical/CRO space.
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