Location
Remote
Job Type
Full-time
Posted
July 15, 2026
Job Description
Informed Consent Writer
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As a Medical Writer I at ICON, you will the development and preparation of clinical trial documents, regulatory submissions, and scientific publications, contributing to the advancement of innovative treatments and therapies.
**What You Will Do:**
Your role will involve delivering medical writing work to a high standard, working closely with your team and stakeholders.
Key responsibilities include:
+ Collaborating with cross-functional teams to prepare, write, and edit clinical study reports (CSRs), clinical protocols, investigator brochures (IBs), patient narratives
+ Conducting literature reviews, data analysis, and interpretation of clinical trial ...
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As a Medical Writer I at ICON, you will the development and preparation of clinical trial documents, regulatory submissions, and scientific publications, contributing to the advancement of innovative treatments and therapies.
**What You Will Do:**
Your role will involve delivering medical writing work to a high standard, working closely with your team and stakeholders.
Key responsibilities include:
+ Collaborating with cross-functional teams to prepare, write, and edit clinical study reports (CSRs), clinical protocols, investigator brochures (IBs), patient narratives
+ Conducting literature reviews, data analysis, and interpretation of clinical trial ...
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