Informed Consent Writer

Clinical Careers Page(1 month ago)

RemoteFull TimeMedior$106,993 - $143,458 (estimated)Clinical Operations

About this role

The Informed Consent Writer at ICON develops clear, health-literate informed consent documents for clinical trials across multiple therapeutic areas, using company tools, templates and systems. The role supports clinical development and global trial operations and ensures patient-facing materials align with regulatory guidance and company standards.

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Required Skills

Health Literacy
Protocol Knowledge
Clinical Trials
Medical Writing
MS Office
Document Management
Project Management
Communication
Regulatory Knowledge
Content Management

Qualifications

Life Sciences Degree
3-5 Years Experience

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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