Informed Consent Writer

Job Summary

Working remotely on a full-time basis, the Informed Consent Writer will prepare informed consent documents for clinical trials using health literate language, ensuring candidates can make informed decisions about participation while collaborating across multiple therapeutic areas.

Key responsibilities

• Read and understand protocol-specific designs, objectives, and study procedures to create informed consent documents
• Collaborate with protocol authors to ensure comprehensive understanding and timely delivery of informed consent documents
• Manage informed consent writing projects, including design, planning, and preparation of documentation in support of clinical development

Required qualifications

• Life sciences degree
• 3-5 years of relevant experience, including experience translating scientific material for a lay audience
• Understanding of clinical trial operations and informed consent forms
• Technical expertise in MS Office and Adobe Acrobat
• Experience with document management systems and collaborative authoring tools