Informed Consent Writer

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

The **Informed Consent Writer (ICW)** is responsible for preparing informed consent documents that disclose information about a clinical trial using health literate language to help a candidate make an informed decision about trial participation. The ICW will work across multiple therapeutic areas using client tools, systems, guidelines, templates, and processes. The ICW is to demonstrate the following skills:

**Scientific Knowledge/Health Literacy**

+ Understanding of protocol structure and knowledge of the relevant information needed to create an informed consent document
+ Understanding of clinical trial operations with specific knowledge of informed consent forms...