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Leads international pharmaceutical congresses and meetings from planning through post-event analysis. Manages delegate logistics, venues, suppliers, budgets, client relationships, compliance, project deliverables, and on-site execution. Provides quality control, resolves issues, monitors profitability, and supports virtual meeting and registration technology. Requires conference management experience in pharmaceutical, clinical research, or healthcare settings, strong communication and organizational skills, proficiency with Microsoft Office, and a bachelor’s degree.

The role involves leading project teams for clinical trials, managing operations, budgets, and ensuring timely delivery to exceed client expectations.

Lead enterprise AI adoption by translating technical AI concepts for non-technical stakeholders, curating AI education and communications, partnering with change management, L&D, and communications, triaging AI requests, and managing a team to build organizational AI fluency and adoption metrics.

As a Regulatory Affairs Consultant, you will provide strategic regulatory guidance for clinical studies, ensuring compliance and efficient trial execution while engaging with health authorities and stakeholders.

This role is responsible for developing global training programs for clinical research, managing course design, and ensuring compliance with regulatory standards while mentoring junior staff.