Overview In this role you lead Phase I clinical projects for a single sponsor, ensuring on-time study delivery within budget and regulatory guidelines. You act as the primary liaison between the sponsor and our company, coordinating cross-functional teams
Overview As a Clinical Research Associate in Real World Late Phase, you monitor and manage trial sites to ensure regulatory compliance and data integrity. You will perform remote and on-site activities across initiation, monitoring, and close-out, collaborating
Overview In this role you drive the design and execution of early-stage oncology clinical development plans, leading cross-functional teams to translate strategy into patient-ready programs. You will shape trials, contribute to regulatory and Medical Affairs strategies,
Overview In this role, you drive early-phase obesity and liver programs from strategy through execution, leading cross-functional teams to advance therapies. You’ll influence regulatory strategy and contribute to Medical Affairs plans, shaping evidence generation and decision-making across