CPC Clinical Research

Support administrative safety management tasks including data entry, report generation, and Trial Master File documentation. Coordinate with investigational sites and sponsors to resolve data queries and ensure timely completion of project deliverables.

Lead the statistical design and execution of clinical studies, including the development of analysis plans and oversight of statistical deliverables. Collaborate with cross-functional teams to ensure regulatory compliance and communicate complex results to stakeholders.

The role focuses on conducting Site Endpoint Evaluation Visits (SEEVs) and providing operational support for international site enrollment and retention. It involves training site staff on data collection, reviewing source documents, and ensuring data quality and compliance.