Clinical Project Manager

Typical Accountabilities - Coordinate lifecycle management, enhancement, and business continuity for Study Delivery processes, systems, reporting, and technology across the clinical research portfolio. - Develop, implement, and continuously improves reporting tools, metrics, and analytical processes, identifying new opportunities for optimization and efficiency. - Lead the delivery of centrally managed study services-such as document management, clinical trial transparency, and system training-to ensure consistency, compliance, and best practice across all drug projects. - Serve as the principal contact for document management activities from initial production/import through completion of the Clinical Study Report and regulatory archiving. - Collaborate with internal stakeholders (Study Delivery, Clinical Development, Data Management, Patient Safety, Compliance) and external partners (service providers, regulatory bodies) to ensure seamless study administration and regulatory compliance. - Facilitate dynamic communication channels to share knowledge, disseminate best practices, and provide guidance and training on current and evolving study systems, standards, and procedures. - Act as a subject matter expert for risk management, contingency planning, and change management, proactively identifying and resolving operational issues or process non-compliance. - Maintain up-to-date awareness of external trends, regulatory requirements, and enabling technologies in clinical trial