Remote Informed Consent Writer for Clinical Trials

A leading clinical research organization is seeking an Informed Consent Writer to prepare informed consent documents for clinical trials. The role involves using health literate language to facilitate candidate understanding. Responsibilities include writing, editing, and managing informed consent projects across therapeutic areas. The ideal candidate will have a life sciences degree and 3-5 years of relevant experience, with outstanding skills in communication and project management. This position offers remote work opportunities, supporting work-life balance. #J-18808-Ljbffr