Arianne brings over 20 years clinical research experience from Phase I, II, III and IV studies in both medical devices and pharmaceutical industries with responsibilities spanning all aspects of clinical research from feasibility, protocol development, study start up, monitoring, study management and medical writing. Roles have included operational and leadership positions including Clinical Affairs Manager, Country Study Manager, Senior CRA.
Ari has held senior roles held with in companies, overseeing clinical research quality and staff training and development, investigator/site engagement, CRO oversight and clinical strategy or pipeline assessment. Extensive experience in developing and introducing new research technologies and systems to departments including quality system development and implementation including CAPA management.