# Informed Consent Specialist

**Company**: ICON
**Work arrangement**: remote
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Mexico-Mexico-City/Informed-Consent-Specialist_JR159899?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_3baccc8c-953

## Description

ICON is a global 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.

**Responsibilities**

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 organisational skills, with the ability to manage multiple document versions and timelines.

- Clear written and verbal communication skills, with a patient-centric approach to document content.

- Proficiency with MS Office and comfort working with document management systems and trackers.

**Rewards & Benefits**

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

- Competitive base salary and performance related incentives

- Health and wellbeing programmes including medical, dental, and vision coverage where applicable

- Retirement and pension plans

- Life assurance and disability coverage

- Employee assistance programmes and wellbeing resources

- Learning and development opportunities through structured training and career pathways

For more fresh new jobs, check out [yubhub.co](https://yubhub.co/).

## Skills

### Required
- informed consent
- clinical research
- regulatory affairs
- document management
- MS Office

### Nice to have
- Spanish

---

Source: [Apply at icon.wd3.myworkdayjobs.com](https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Mexico-Mexico-City/Informed-Consent-Specialist_JR159899?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)