Informed Consent Writer
Job Summary
Working remotely, the part-time Informed Consent Writer will prepare informed consent documents for clinical trials using health literate language, ensuring candidates can make informed decisions regarding trial participation while collaborating across multiple therapeutic areas.
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, ensuring timely delivery and compliance with guidelines
Required qualifications
- Life sciences degree
- 3-5 years of relevant experience, including expertise in translating scientific material for a lay audience
- Understanding of clinical trial operations and informed consent documentation
- Technical expertise in MS Office and Adobe Acrobat
- Experience with document management systems and collaborative authoring tools
Complete Job Description
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