ICON seeks an Informed Consent Specialist to support the development, review, and management of informed consent documents for clinical research. The role ensures compliance with regulations and protocols while maintaining patient-focused, clear documentation across multiple countries.
Responsibilities
Prepare and review informed consent forms in accordance with protocols, regulations, and sponsor requirements
Coordinate collection and tracking of ethics committee and regulatory approvals for consent documents
Manage consent templates, translations, and version control across multiple countries and sites
Liaise with internal teams to address questions regarding consent language and requirements
Ensure accurate filing and documentation to maintain audit and inspection readiness
Requirements
Bachelor's degree in life sciences, healthcare, legal studies, or related field
Initial experience in clinical research, regulatory affairs, ethics submissions, or document management
Basic understanding of informed consent principles, GCP, and ethical requirements
Strong attention to detail and organisational skills with document version management ability
Clear written and verbal communication skills with patient-centric approach
Proficiency with MS Office and document management systems