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 improve 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 a...