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

What You Will Do:
You will take responsibility for clinical research deliverables, applying your skills to ensure quality and efficiency.

What you will be doing:
• Performs routine reviews of clinical and third-party data for subjects enrolled in clinical research protocols based on edit check/output specification documentation
• Maintains clinical data management related study documentation as appropriate
• May be responsible for local lab data entry and local lab data review activities as required




• Executes data review and analytic requirements on low to medium complexity work
• Manages third-party data reconciliation process
• Assist Clinical Data Science Lead in development of eCRF, Data Validation Specifications, and Study Specific Procedures

Your profile:
• 1-2 years of clinical data management experience in a clinical research organization or pharmaceutical company
• Basic knowledge of the drug development process
• Knowledge of at least 1 Clinical Data Management System (Medidata RAVE, InForm, Veeva, etc.)
• Strong knowledge of computerized information systems and standard application software (Windows, MS Office)
• Excellent written and oral communication skills
• Bachelor’s degree or local equivalent
• Equivalent combination of education, training, and relevant experience may be considered in place of the education and experience stated above. All employees must read, write, and speak fluent English and host country language.

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📌 CDC I (Ciudad de México)
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📍 Ciudad de México