Clinical Research Associate
Regular, Full Time
Australia, Sydney
Your role as a Clinical Research Associate will sit within the Global Drug Development Team, responsible for the successful delivery and conduct of TMO global studies in accordance with ICH- GCP, SOPs, and local regulations.
Your responsibilities include, but are not limited to:
• Manage assigned studies and sites from start-up through to archiving
• Work with the medical experts and their teams to meet study deliverables (start-up timelines, patient recruitment targets, DBL)
• Liaise and collaborate with Novartis colleagues to ensure global studies are placed within Australia and New Zealand
• Ensure delivery of quality data through completion of clinical trials
Ann: Mesoblast Corporate Update Webcast, page-112
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