Informed Consent Writer

Clinical Careers Page(1 month ago)

RemoteFull TimeMedior$101,986 - $136,968 (estimated)Medical Writing

About this role

The Informed Consent Writer prepares informed consent documents for clinical trials using clear, health-literate language to help candidates make informed participation decisions. The role supports multiple therapeutic areas and uses company tools, systems, templates and regulatory guidance to produce study-specific consent materials. This position contributes to clinical development by ensuring consent documentation meets regulatory and health-literacy standards.

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Required Skills

Informed Consent
Health Literacy
Protocol Knowledge
Clinical Trials
MS Office
Adobe Acrobat
Document Management
Authoring Tools
Content Management
Project Management

+2 more

Qualifications

Life Sciences Degree

About Clinical Careers Page

iconplc.com

ICON plc is a global clinical research organisation (CRO) that provides outsourced clinical development and commercialisation services to pharmaceutical, biotechnology and medical device companies. It offers end-to-end drug and device development support — including clinical trial management across phases, data management and biostatistics, regulatory and safety/pharmacovigilance, and commercialisation and market-access services. ICON combines scientific and therapeutic expertise with technology and a scalable global operations network to accelerate development and bring therapies to patients. Clients engage ICON for integrated, experienced CRO support across the full product lifecycle.

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