Informed Consent Specialist II

Clinical Careers Page(3 months ago)

HybridFull TimeMedior$0 - $0Clinical Operations

About this role

ICON is hiring an Informed Consent Form (ICF) Specialist to ensure accuracy, compliance, and timely approval of informed consent documents for clinical trials. The role supports global and country-specific ICF/SIS development, interacts with ethics committees and regulatory authorities, and contributes to the ethical conduct and successful initiation of studies.

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Required Skills

ICF Writing
Informed Consent
ICH/GCP
Regulatory Knowledge
Stakeholder Collaboration
Query Resolution
Timeline Management
Documentation Archiving
Mentoring
Protocol Interpretation

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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