Informed Consent Specialist I - Homebased - Colombia and Chile

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 an Informed Consent Specialist II at ICON, you will support the development, review, and management of informed consent documents to ensure they are clear, compliant, and patient-focused.

**What You Will Do:**

You will take responsibility for clinical research deliverables, applying your skills to ensure quality and efficiency.

Key responsibilities include:

+ Responsible for the preparation and review of informed consent forms (ICFs) in accordance with protocols, regulations, and sponsor requirements.
+ Coordinating the collection and tracking of ethics committee and regulatory approvals related to informed co...