Informed Consent Writer

Clinical Careers Page(24 days ago)

RemoteFull TimeMedior$107,674 - $144,037 (estimated)Medical Writing

About this role

An Informed Consent Writer at ICON prepares health-literate informed consent documents that translate clinical trial information into clear materials for potential participants. The role supports multiple therapeutic areas, leveraging client tools, templates and regulatory guidance to ensure documents meet applicable standards. This is a remote position within ICON’s clinical research/medical writing organization.

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Required Skills

Protocol Knowledge
Health Literacy
Medical Writing
Project Management
MS Word
Excel
Adobe Acrobat
Document Management
Communication
Time Management

+3 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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