Informed Consent Specialist I (Ciudad de México)

Informed Consent Specialist I (Ciudad de México)

06 sep
|
IRE
|
Ciudad de México

06 sep

IRE

Ciudad de México

Informed Consent Specialist I - Mexico - Homebased
ICON is a general 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 attenti

📌 Informed Consent Specialist I (Ciudad de México)
🏢 IRE
📍 Ciudad de México

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