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

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