Clinical Data Coordinator II

ICON Clinical Research; México; Hybrid; MXN 1.318.000 - 1.883.000; Vollzeit

Benefits dieser Stelle

Annual leave entitlements

Health insurance options

Retirement planning options

Global Employee Assistance Programme (

Life assurance

Country-specific benefits

Zusammenfassung

ICON Clinical Research is seeking a Clinical Data Coordinator II to design and analyze clinical trial data in Mexico and Colombia. You will work with your team to deliver data management tasks and ensure high data quality across studies.

You will collaborate with cross-functional teams, maintain strict data governance, and contribute to the advancement of therapies by ensuring accurate data capture and validation in a fast-paced environment.

Qualifikationen

• Bachelor's degree in Life Sciences or Healthcare is required.
• Experience in clinical data management within pharma/biotech.
• Familiarity with data management software such as Medidata or Oracle RDC.
• Strong attention to detail and ability to work in a fast-paced environment.
• Excellent communication and collaboration with cross-functional teams.
• Knowledge of regulatory guidelines (ICH-GCP) is a plus.

Aufgaben

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

Kenntnisse

Clinical data management

Attention to detail

Communication skills

Regulatory knowledge (ICH-GCP)

Cross-functional collaboration

Ausbildung

Bachelor's degree in Life Sciences or Healthcare

Tools

Medidata

Oracle RDC

Jobbeschreibung

Clinical Data Coordinator II - Mexico and Colombia

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 a CDC II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

Your role will involve delivering clinical data management work to a high standard, working closely with your team and stakeholders.

Key responsibilities include:

• 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:

You will bring relevant clinical data management experience, along with the following qualifications and skills.

Required qualifications and experience:

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

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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 (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)