clinical data coordinator position responsible for reviewing clinical trial data, maintaining study documentation, and supporting data management activities. Requires 1-2 years of clinical data management experience and proficiency with clinical data systems.

responsibilities

- review clinical and third-party data for enrolled study subjects against edit checks and specifications
- maintain and organize clinical data management documentation as needed
- conduct local laboratory data entry and review activities when required
- execute data review and analysis for low to medium complexity assignments
- manage reconciliation of third-party data and support ecrf development

requirements

- 1-2 years of clinical data management experience in cro or pharmaceutical settings
- basic understanding of drug development processes
- proficiency with at least one clinical data management system (medidata rave, inform, veeva)
- strong computer skills including windows and microsoft office
- excellent written and verbal communication abilities
- bachelor's degree or equivalent
- fluent english and host country language proficiency

📌 Cdc i (Ciudad de México)
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📍 Ciudad de México