Informed Consent Specialist (Level Ii And Senior)

Icon; A distancia; MXN 1,074,000 - 1,522,000; Jornada completa

Descripción de la vacante

A leading clinical research organization is looking for a Senior Informed Consent Specialist to develop and review ICFs, ensuring compliance with regulations. In this homebased position, you will collaborate with various stakeholders and mentor new hires. The candidate should have 3+ years of ICF writing experience and strong English communication skills. ICON offers competitive benefits and supports a diverse and inclusive culture that fosters innovation.

Servicios

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

Global Employee Assistance Programme

Flexible optional benefits

Formación

• 3+ years of experience in ICF writing/development.
• Proficient knowledge of ICH/GCP guidelines and country regulations related to Informed Consent.
• Ability to effectively communicate with diverse stakeholders.

Responsabilidades

• Developing and reviewing ICFs and SIS for global and site-specific needs.
• Ensuring compliance with ICON SOPs and country regulations.
• Mentoring and coaching new hires.

Conocimientos

Strong English writing and communication skills

Analytical and problem-solving skills

Collaborative team player

Descripción del empleo

Senior Informed Consent Specialist - Homebased - Mexico

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. We’re currently seeking a Senior Informed Consent Form (ICF) Specialist to join our diverse and dynamic team.

What you’ll be doing

• Developing and reviewing ICFs: preparing, reviewing, and approving Subject Information Sheets (SIS) and ICFs for global master templates, country‑specific versions, and site‑specific adaptations.
• Ensuring compliance: applying proficient knowledge of ICON SOPs/WPs, ICH/GCP guidelines, and applicable country regulations related to Informed Consent requirements.
• Stakeholder collaboration: serving as a key point of contact for Sponsors, SSU Project Managers, Clinical Trial Managers, and other functional leads to optimize performance and ensure successful project outcomes.
• Query resolution: reviewing, negotiating, and approving all Ethics Committee (EC), Institutional Review Board (IRB), and Competent Authority (CA) queries related to country and site‑specific ICFs.
• Timeline management: forecasting and tracking SIS & ICF approval timelines, proactively identifying risks, and developing contingency plans to mitigate potential impacts.
• Knowledge leadership: acting as a Subject Matter Expert (SME) for assigned topics, staying updated on changing regulatory and language requirements affecting ICFs, and developing/conducting training.
• Documentation and archiving: ensuring the accuracy and completeness of ICF documents transferred for filing into the Trial Master File (TMF).

Mentorship & Representation

• Mentoring and coaching new hires during their onboarding process.
• Representing the department at audits, inspections, and on various committees and work groups.

Your profile

3+ years of experience in ICF writing/development. Strong English writing and communication skills are required. Proficient knowledge of ICH/GCP guidelines and applicable country regulations related to Informed Consent. Ability to work collaboratively in a team environment and effectively communicate with diverse stakeholders. Strong analytical and problem‑solving skills, with excellent attention to detail. Protocol interpreting & review is preferred, but not required.

What ICON can offer you

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well‑being and work‑life balance opportunities for you and your family.

Benefits

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family's needs
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, LifeWorks, offering 24‑hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well‑being
• Life assurance
• Flexible country‑specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values.

Equal Opportunity and Accessibility

We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.

Application

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there's every chance you're exactly what we’re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply#J Ljbffr