Data Coordinator

ICON; Ciudad de México; Presencial; MXN 200,000 - 400,000; Jornada completa

Descripción de la vacante

A world-leading healthcare organization in Mexico City is seeking a Data Coordinator to manage clinical trial data integrity and support study design. The ideal candidate will have a relevant degree and experience in clinical research. This role offers competitive salary and a range of benefits focused on well-being and work-life balance.

Servicios

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Life assurance

Flexible optional benefits

Formación

• Bachelor's degree in a relevant field, such as life sciences, healthcare, or information management.
• Previous experience in clinical research or data coordination preferred.
• Strong attention to detail and organizational skills.
• Proficiency in data management software and tools.
• Excellent communication and teamwork abilities, with the ability to work effectively in a fast-paced environment.

Responsabilidades

• Collaborating with cross-functional teams to develop data collection protocols and tools.
• Overseeing the collection, entry, and verification of clinical trial data.
• Performing quality checks to ensure data accuracy, completeness, and compliance with regulatory requirements.
• Generating and distributing reports on data collection and management activities.
• Supporting data analysis and interpretation efforts as needed.

Descripción del empleo

Data Coordinator

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 are currently seeking a Data Coordinator to join our diverse and dynamic team. As a Data Coordinator at ICON, you will play a pivotal role in managing and maintaining the integrity of clinical trial data, supporting the design and analysis of studies, and contributing to the advancement of innovative treatments and therapies.

Responsibilities

• Collaborating with cross-functional teams to develop data collection protocols and tools
• Overseeing the collection, entry, and verification of clinical trial data
• Performing quality checks to ensure data accuracy, completeness, and compliance with regulatory requirements
• Generating and distributing reports on data collection and management activities
• Supporting data analysis and interpretation efforts as needed

Requirements

• Bachelor's degree in a relevant field, such as life sciences, healthcare, or information management
• Previous experience in clinical research or data coordination preferred
• Strong attention to detail and organizational skills
• Proficiency in data management software and tools
• Excellent communication and teamwork abilities, with the ability to work effectively in a fast-paced environment

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 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, subsidized travel passes, health assessments, among others

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.

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.