Clinical Data Coordinator II

ICON Clinical Research; Ciudad de México; Híbrido; MXN 200,000 - 400,000; Jornada completa

Descripción de la vacante

A leading clinical research organization is seeking a Clinical Data Coordinator II to support data management tasks in a hybrid work environment in Mexico City. The ideal candidate will have a Bachelor's degree in a relevant field, a strong attention to detail, and intermediate experience in clinical data management. Responsibilities include assisting in data maintenance, managing data reconciliation, and addressing data queries. This role offers a competitive salary along with a range of benefits designed for well-being and work-life balance.

Servicios

Health insurance offers

Annual leave entitlements

Retirement planning offerings

Global Employee Assistance Programme

Flexible optional benefits

Formación

• At least 1-3 years of experience managing clinical data bases.
• Intermediate knowledge of clinical data management within pharmaceutical or biotechnology.

Responsabilidades

• Assist Data Management Study Lead in data maintenance.
• Manage clinical and third-party data reconciliation.
• Communicate status of study and task metrics to the project team.
• Address data-related questions and recommend solutions.
• Identify root causes to resolve data issues.

Conocimientos

Attention to detail

English (advanced)

Communication

Collaboration

Educación

Bachelor's degree in Life Sciences or Healthcare

Herramientas

RAVE

Veeva

Inform

Descripción del empleo

CDC II - Mexico City

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.

Clinical Data Coordinator II

This is a hybrid role requiring 3 days in the office and 2 days working from home.

Location: Mexico City - Insurgentes Sur

What you will be doing

• Assist Data Management Study Lead in maintenance of eCRF, Data Validation Specifications, and Study Specific Procedures.
• Manage clinical and third-party data reconciliation based on edit specifications and data review plans.
• Tracks and communicates status of study and task metrics to clinical data scientist, project team, and functional management.
• Address data related questions and recommend potential solutions.
• Identify root cause to systematically resolve data issues.

Your profile

• Bachelor's degree in a relevant field, such as Life Sciences or Healthcare.
• English advanced.
• Intermediate knowledge of clinical data management within the pharmaceutical or biotechnology industry.
• At least 1-3 years of experience managing clinical data bases (RAVE preferido, Veeva, Inform)
• Strong attention to detail and the ability to work effectively in a fast-paced environment.
• Excellent communication skills and the ability to collaborate with cross‑functional teams.

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.

Our benefits examples include:

• 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 (https://careers.iconplc.com/benefits) to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. 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 (https://careers.iconplc.com/reasonable-accommodations)

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 (https://wd3.myworkday.com/icon/d/task/1422%241235.htmld) to apply