Informed Consent Writer

Job Summary

A company is looking for an Informed Consent Writer to prepare informed consent documents for clinical trials.

Key Responsibilities

• Read and understand protocol-specific design, objectives, and study procedures
• Prepare study-specific informed consent documents using established templates and required risk language
• Manage informed consent writing projects and participate in clinical trial team meetings to ensure timely delivery

Required Qualifications

• Life sciences degree
• 3-5 years of relevant experience preferred, including experience translating scientific material for a lay audience
• Technical expertise in MS Office and Adobe Acrobat
• Experience with document management systems and collaborative authoring tools
• Understanding of ICH and regulatory guidance pertaining to informed consent