Day-to-day management of the conduct of clinical investigations at study sites as a representative of the ADC Clinical Affairs team
Monitoring to ensure studies are conducted according to protocols, applicable ADC procedures, GCP and all applicable regulations, and to ensure that subject safety and data integrity are maintained
Support cross-functional projects and liaise with other groups across Abbott. Provide input into new product development projects, execute clinical activities to progress both studies and projects
Conduct site visits and study monitoring to ensure all clinical studies meet procedural and GCP requirements
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