ICON plc

Informed Consent Writer

ICON plc

8 days ago
Remote
Full Time
Medior
0 applicants
ICON plc
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About this role

ICON plc is seeking an Informed Consent Writer to prepare clear, health-literate informed consent documents for clinical trials across various therapeutic areas. The role involves working with protocols, using client tools and systems, and ensuring compliance with regulatory guidelines to support clinical development.

Skills

Qualifications

Life sciences degree
ICON plc

About ICON plc

iconplc.com

Industries

Healthcare, Consulting, Technology

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.

About ICON plc

Headquarters

San Francisco, CA

Company Size

201-500 employees

Founded

2018

Industry

Technology

Glassdoor Rating

4.2 / 5

Leadership Team

Sarah Johnson

Chief Executive Officer

Michael Chen

Chief Technology Officer

Emily Williams

VP of Engineering

David Rodriguez

VP of Product

Jessica Thompson

Chief Financial Officer

Andrew Park

VP of Sales

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