Senior CDC

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

Descripción de la vacante

A leading healthcare organization in Mexico is seeking a Senior Clinical Data Coordinator to join their dynamic team. You will manage clinical data for trials, ensuring quality and compliance while mentoring junior coordinators. The ideal candidate has a relevant degree and 3+ years in clinical data management. This role offers a competitive salary and a range of comprehensive benefits to support work-life balance and family welfare.

Servicios

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Flexible optional benefits

Formación

• 3+ years experience in clinical data management within the pharmaceutical or biotechnology industry.
• Familiarity with data management software and systems.
• Knowledge of regulatory guidelines and standards (e.g., ICH-GCP) is a plus.

Responsabilidades

• Create and maintain detailed data management plans and documentation.
• Participate in the identification and resolution of data discrepancies.
• Collaborate closely with cross-functional teams.

Conocimientos

Attention to detail

Communication skills

Data management

Problem solving

Educación

Bachelor's degree in Life Sciences or Healthcare

Herramientas

Medidata

Oracle RDC

Descripción del empleo

Senior CDC - 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 are currently seeking a Senior Clinical Data Coordinator to join our diverse and dynamic team. As a Clinical Data Coordinator at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

• Create and maintain detailed data management plans and documentation, ensuring compliance with industry standards and regulatory requirements.

• Participate in the identification and resolution of data discrepancies and issues, working to streamline data flow and enhance data quality throughout the study lifecycle.

• Collaborate closely with cross-functional teams, including clinical operations and biostatistics, to develop and execute data management strategies tailored to specific studies.

• Perform other project activities as required in order to ensure that study timelines are met (for example, filing and archiving of study documentation , dispatching of queries to investigator sites for resolution, etc.).

• Mentor junior data coordinators, providing expert guidance on data reconciliation, coding, and cleaning procedures.

Your profile

• Bachelor's degree in a relevant field, such as Life Sciences or Healthcare.

• 3+ years experience in clinical data management within the pharmaceutical or biotechnology industry.

• Familiarity with data management software and systems (e.g., Medidata, Oracle RDC, or similar).

• 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.

• Knowledge of regulatory guidelines and standards (e.g., ICH-GCP) is a plus.

#LI-FB2

#LI-Homebased

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, subsidized 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. 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

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