Conduct strategic environmental surveillance in oncology to anticipate regulatory and operational changes affecting sites and R&D in the United States.
Provide insight to leadership on site landscape trends, operational risks, and emerging engagement models.
Lead the development and expansion of a US oncology site network spanning academic centers, community practices, and emerging site models.
Enhance collaboration between sites and GSK clinical teams to improve performance and resolve obstacles during site start‑up and study execution.
Create and implement strategic partnership models and frameworks for clinical sites.
Build and nurture relationships with community sites, engaging local investigators and staff to expand the GSK partnership network.
Provide strategic input for operational excellence, process efficiency and trial delivery both internally and externally.
Identify and disseminate best practices and contribute to standardization across local operations.
Track compliance with site partnership agreements, pinpoint problem areas, and take corrective actions.
Drive performance, by putting in place mutually agreed KPIs (quality and performance) and organizing periodic review with external partners.
Requirements
Bachelor's degree in related discipline, preferably in life science.
5 + years' experience in clinical research operations.
3 + years' experience in Oncology clinical research.
Benefits
health care and other insurance benefits (for employee and family)