Informed Consent Specialist (Level II and Senior)

Clinical Careers Page(2 months ago)

RemoteFull TimeSenior$139,983 - $188,077 (estimated)Clinical Operations

About this role

A Senior Informed Consent Specialist at ICON is a senior clinical research professional working homebased from Mexico to support the ethical and regulatory aspects of clinical studies. The role focuses on informed consent documentation for global, country-specific, and site-specific trials and serves as a subject matter expert on consent requirements and regulatory expectations. This position liaises with cross-functional stakeholders to support study initiation and regulatory compliance.

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Required Skills

ICF Writing
Regulatory Compliance
ICH/GCP
Document Review
Stakeholder Collaboration
Timeline Management
Mentorship
Audit Representation
English Communication

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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