Responsible for coordinating the operational and strategic aspects for Clinical Trial Submissions

Essential Functions

• Lead the submission process from strategy formation to clinical trial approval
• Coordinate creation of trial submissions strategy development, planning and delivery
• Responsible for Quality checks on CTIS before submissions
• Financial planning and tracking
• Driving discussions, consolidating inputs from stakeholders and facilitating CTR submission strategy
• Responsible for coordinating submissions in the CTIS portal

Qualifications

• 3 to 5 years experience building RDC databases in support of clinical research
• Experience in regulatory and submissions
• Project management skills

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com