Lead regulatory projects focusing on RIM system implementations, IDMP readiness, and data quality for pharmaceutical and life sciences companies. Manage project timelines, budgets, and stakeholder expectations while mentoring consultants and contributing to business growth.
Lead the design, optimization, and digitalization of Quality Management Systems (QMS) for leading pharmaceutical and life sciences companies. Manage complex projects from analysis and conception through to implementation and go-live on platforms like Veeva Vault Quality.
Lead regulatory projects and teams to implement best practices and digital transformation within the life sciences sector. Act as a liaison between the company and software providers to improve business processes and ensure regulatory compliance.
