Regulatory Coordinator

Responsibilities:

• Support vendor related activities including review of contracts, qualification documents for inherited vendors, creation of excel file overview/summaries, follow up on descoping/scoping activities.
• Project Management activities for assigned projects/ track and follow up on actions.
• Overseeing and managing Vendor Management systems, processes, and supporting Vendor Management activities related to Integrations.
• Preparation and completion of vendor management forms & assessment to support integration.
• Interaction with assigned vendors & NVS organizations/ acquired company to collect the as is model and support the “to be” model.

Work Experience:

• Project Management experience
• Knowledge of clinical trials, regulatory submissions, and vendor management
• Collaborating across boundaries

Skills:

• Organizational skills
• Proactive approach
• Proficiency in project management, and project planning
• Detailed oriented
• Fluent in English
• Valid working license for the country of application

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. 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