Informed Consent Specialist - Homebased - Mexico and Colombia
ICON is a integral healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As an Informed Consent Specialist I 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:
Assisting in 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 consent documents.
Supporting the management of consent templates, translations,
and version control across countries and sites.
Liaising with internal teams to address basic questions and clarifications regarding consent language and requirements.
Ensuring accurate filing and documentation of informed consent materials to maintain audit and inspection readiness.
Contributing to process improvements and standardisation efforts within the informed consent function.
Your Profile:
You will bring relevant clinical research experience, along with the following qualifications and skills.
Required qualifications and experience:
Bachelor's degree in life sciences, healthcare, legal studies, or a related field, or equivalent experience.
Initial experience in clinical research, regulatory affairs, ethics submissions, or document management is preferred.
Basic understanding of informed consent principles, GCP, and ethical requirements, with a willingness to learn.
Strong attention to detail and
📌 Informed Consent Specialist (Xico)
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