As a CTA will play a key role in supporting the management and execution of clinical trials by handling a range of administrative and operational tasks. You will contribute to the smooth execution of clinical trials through efficient coordination, documentation, and communication with various stakeholders.
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Performs data review of clinical trial data, including query management, and reconciliation review of external data against EDC data. May assist in creating study documents or running study reports and metrics. Files study documentation in electronic Trial Master File (eTMF) and department project files. Assists with quality review of activities performed by the CRO, as needed, and ensures compliance with own Learning Curricula, corporate and/or GXP requirements.