Clinical Data Coordinator I - Mexico City (Hybrid) & Colombia (Remote)
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 have an incredible opportunity for a Clinical Data Coordinator I to join ICON’s Full Service IOD Clinical Data Science team. The CDC I supports and executes the data review activities that contribute to delivery of clinical data that meets agreed upon data integrity standards.
Locations:
- Mexico City (office-based an average of 3 days per week)
- Colombia (home-based or hybrid)
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 spea
📌 Clinical Data Coordinator I (Bogotá)
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📍 Bogotá