Clinical Project Manager

Accomplished, dynamic professional experienced in synergizing communications between clinical research centers, contract research organizations (CROs), and major pharmaceutical corporations to amass clinical investigation objectives. Adept at executing, managing and monitoring IRB-approved, Phase I-III clinical studies and data management. Proven success in identifying opportunities to improve timely event reporting, increase protocol compliance, and streamline data processes preceding database lock. Make certain that all research initiatives align with key business goals and critical growth objectives. Dedicated and resourceful leader who thrives in fast-paced, deadline-driven environments and excels in adapting to unforeseen challenges, shifting priorities, and changing responsibilities. Independently master and apply new skills to advance study activities, improve accuracy and reliability of data. Valued professional recognized for exemplary performance, exceptional communication skills, and high professional standards.

Clinical Research