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ICON plc
Overview
The Informed Consent Writer is responsible for creating health-literate informed consent documents for clinical trials across various therapeutic areas. This includes collaborating with protocol authors and managing the design and planning of documentation to ensure timely delivery and regulatory compliance.
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Compensation
Salary not listed
Posted
22 days ago
bioMérieux
Develop and manage scientifically sound documents, including manuscripts and posters, to communicate complex clinical data to healthcare professionals. Lead publication planning and ensure all materials comply with ethical guidelines and regulatory policies.
$95,000 - $124,000 / YEAR
23 days ago
