Clinical Data Coordinator II
Core
Design and analyze clinical trials by interpreting complex medical data to support the development of new medicines and treatments.
Role type
Clinical Data Coordinator (IC)
Builds
Clinical trial data packages and study deliverables for pharmaceutical and biotechnology clients.
Domain
Healthcare / Clinical Research / Data Management
Deliverable
production ML models | product features | dashboards & analysis | client delivery
Required skills
Clinical data management, eCRF development, data validation, query management, regulatory guidelines knowledge (ICH-GCP), data management software proficiency
Preferred skills
Knowledge of regulatory guidelines and standards (e.g., ICH-GCP)
Technologies
Medidata, Oracle RDC
Responsibilities
Assist in development of eCRF, Data Validation Specifications, and Study Specific Procedures; Review clinical and third-party data based on edit specifications; Issue clear, accurate, and concise queries to investigational sites; Perform project activities to ensure study timelines are met (e.g., filing, archiving, dispatching queries)
Seniority
Junior to Mid-level, hands-on IC
