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Medical Writer, Scientific Research, Healthcare Content Specalist
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Regulatory Affairs
Self Employed • Temps plein
May 2025 - Present • 1 yr 2 mos
• Prepare and review pharmaceutical regulatory documentation. • Perform scientific literature searches and evidence-based research. • Develop drug monographs, research summaries, and healthcare documents. • Review ACTD/CTD documentation and product information. • Support medical writing and regulatory compliance activities.