Health-Literate Clinical Consent Writer
ICON
ICON is looking for an Informed Consent Writer based in California to prepare informed consent documents for clinical trials. This role requires strong project management skills and a life sciences degree, along with 3-5 years of relevant experience. The candidate will work collaboratively to produce clear, health-literate documents that aid participants in making informed decisions. ICON offers a diverse range of health benefits and emphasizes inclusion and belonging in its corporate culture. #J-18808-Ljbffr ICON
Vacancy posted 1 day ago
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