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Data Coordinator
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- The Data Coordinator is responsible for monitoring the completeness and accuracy of clinical trial data while entering subject source data into Electronic Data Capture (EDC) systems and paper formats.
- Individuals in this role ensure the timely entry of excellent quality data into data capture systems and provide related feedback to the clinical research team to support continuous improvement of training and systems.
- Adhere to International Council on Harmonization - Good Clinical Practice (ICH-GCP) guidelines and Charter Research Standard Operating Procedures (SOPs).
- Adhere strictly to the study protocols and their associated data entry standards, utilizing the Electronic Case Report Form (eCRF) guidelines and data capture snapshots provided by the sponsor, CRO, and EDC vendor.
- Communicate issues with clinical study data to the appropriate Clinical Research Coordinator, Clinical Team Lead, Physician Investigator, Finance Associate and Clinic Manager.
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