Global Regulatory Project Lead

IQVIA; Durham (NC); On-site; USD 97,000 - 271,000; Full time

Job summary

IQVIA is seeking a regulatory professional to support global development programs within the Global Regulatory Science organization. The role focuses on translating regulatory strategy into integrated plans and managing milestones, risks, and deliverables across early- and late-stage development.

Ideal candidates will bring substantial pharmaceutical/biotech regulatory experience, strong program management skills, and the ability to work across a matrixed global organization and with senior

Qualifications

• Significant pharmaceutical/biotech regulatory experience.
• Experience supporting regulatory strategy and execution across development stages, major submissions, global registrations.
• Strong project and program management capabilities for complex timelines and cross-functional deliverables.

Responsibilities

• Support global regulatory development programs across multiple regions (US, EU, Canada, Australia, UK).
• Partner with Global Regulatory Leads and cross-functional stakeholders to translate strategy into executable plans and manage milestones, timelines, risks, and deliverables.
• Support governance, meeting planning/facilitation, and stakeholder communication in global regulatory subteams.

Skills

Regulatory affairs

Regulatory program management

Project management

Communication

Facilitation

Tools

Smartsheet

Veeva RIM

MS Office / PPT timelines

Job description

IQVIA is seeking a regulatory professional to support global development programs within the Global Regulatory Science organization. The role focuses on translating regulatory strategy into integrated plans and managing milestones, risks, and deliverables across early- and late-stage development.

Ideal candidates will bring substantial pharmaceutical/biotech regulatory experience, strong program management skills, and the ability to work across a matrixed global organization and with senior