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Manage Clinical Operations staff, oversee project work assignment, ensure compliance with SOPs, and develop training plans while monitoring performance metrics.

The CRA II position involves working collaboratively to support clinical trial activities, ensuring compliance with protocols, and addressing challenges in a dynamic environment.

Perform site qualification, monitoring, and management, ensuring compliance with regulatory requirements and protocol. Maintain accurate documentation and support project objectives through effective communication and site liaison.

The CRA II is responsible for site qualification, monitoring, management, and ensuring compliance with regulatory and clinical standards throughout the study lifecycle.

The CRA II performs site management duties including site qualification, monitoring, and close-out visits while ensuring compliance with clinical regulations and guidelines.

The CRA II/ SCRA conducts site evaluations, monitors compliance with protocols, and ensures accuracy in clinical data collection while supporting clinical study processes.

The Senior Project Specialist manages project files, handles financial reports, leads meetings, tracks KPIs, supports audits, and trains junior specialists. They serve as a key customer contact and ensure compliance with guidelines.

The CRA II role involves collaborating in clinical studies, engaging with diverse teams, and driving customer success in biopharmaceutical solutions.