Our client, a pharmaceutical company, is seeking a Clinical Research Associate to support the planning, execution, and monitoring of clinical trials at their State College facility. This role works closely with investigators, site staff, and internal quality teams to ensure studies are conducted in compliance with protocol requirements and regulatory standards.
The Clinical Research Associate will manage assigned trial sites, review study documentation, and track progress against enrollment and data collection timelines. This position requires regular site visits, close attention to regulatory detail, and clear communication with cross-functional teams including data management, regulatory affairs, and clinical operations.
This is a full-time, on-site position offering the opportunity to work on a range of therapeutic areas within a structured clinical development environment.
Job Type: Full-Time | Work Type: On-Site | Industry: Pharmaceutical | Experience: Mid-Senior
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