Associate Director, Pharmacovigilance (US)

Worldwide Clinical Trials; Durham (NC); On-site; USD 140,000 - 190,000; Full time

Job summary

Worldwide Clinical Trials is seeking an Associate Director, Pharmacovigilance to lead global safety operations, ensuring patient safety, regulatory compliance, and high-quality pharmacovigilance services across development programs. You will guide teams across therapeutic areas and phases, driving efficiency and outcomes in a dynamic CRO environment.

You will partner with stakeholders worldwide to shape strategy, processes, and technology, while mentoring staff and advancing safety governance

Responsibilities

• Provide strategic and operational oversight of pharmacovigilance projects and staff.
• Partner with global stakeholders to drive quality, efficiency, and continuous improvement in safety operations.
• Contribute to evolution of department processes, technology, and talent development.
• Serve as a trusted advisor to clients and internal teams on global safety requirements and best practices.

Job description

Join a global Contract Resource Organization (CRO) where innovation meets purpose. At Worldwide Clinical Trials, we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are empowered to think creatively, take ownership, and deliver meaningful work that helps bring life-changing therapies to patients around the world.

With more than 4,000 professionals across the globe, we foster a collaborative and inclusive environment where diverse perspectives are valued, growth is encouraged, and every contribution makes an impact. Whether you're building your career or bringing years of experience, you'll have the opportunity to learn, grow, and help shape the future of clinical research.

Make an Impact as an Associate Director, Pharmacovigilance at Worldwide

As an Associate Director, Pharmacovigilance, you will play a critical leadership role in delivering high-quality global pharmacovigilance services that support clinical development programs across a variety of therapeutic areas and trial phases. Your expertise will help ensure patient safety, regulatory compliance, and operational excellence while guiding teams through complex safety reporting challenges.

In this role, you will provide strategic and operational oversight of pharmacovigilance projects and staff, partnering with global stakeholders to drive quality, efficiency, and continuous improvement. You will also contribute to the evolution of department processes, technology, and talent development while serving as a trusted advisor to clients and internal teams on global safety requirements and best practices.

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