PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Their customers include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 46 countries and approximately 23,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to help customers bend the cost and time curve of drug development to deliver life-changing therapies that improve health.

Pharmaceutical

Research

PPD's headquarters in Wilmington, NC, United States

David Simmons

Rob P.

Matthew Bush

Claire Revell

Keri Henderson

Michael Wingerter

Graeme Cuthbertson

Judy Isenberg

The Clinical Research and Data Management team at PPD is responsible for designing, implementing, and managing clinical trials to ensure they meet regulatory standards and deliver reliable data. This team collaborates closely with clinical sites, monitors trial progress, and oversees data collection and analysis, ultimately facilitating the successful development of new therapies for clients in the pharmaceutical and biotech industries. Their commitment to quality and innovation helps streamline the drug development process and improve patient outcomes.

Clinical Research and Data Management

The Leadership Team at PPD is responsible for setting the strategic direction and overarching vision of the company, ensuring the effective management and integration of global operations across various regions and therapeutic areas. This team collaborates closely to foster innovation, enhance operational excellence, and drive business development, while maintaining a strong commitment to quality and efficiency in drug development services. They play a vital role in navigating complex challenges in the pharmaceutical landscape and aligning resources to deliver impactful therapies to customers and patients worldwide.

Leadership Team

The Medical Writing and Regulatory Affairs team at PPD is responsible for the creation and management of crucial documentation required for regulatory submissions and compliance. This team collaborates closely with clinical and safety experts to produce high-quality clinical study reports, safety narratives, and regulatory filings, ensuring that all written materials meet stringent industry standards and support the timely development and approval of life-changing therapies. Their expertise in pharmacovigilance and regulatory requirements helps clients navigate the complexities of the drug development process.

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PPD

Org chart

Teams

Clinical Research and Data Management

Leadership Team

Medical Writing and Regulatory Affairs

Offices

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PPD

Org chart

Teams

Clinical Research and Data Management

Leadership Team

Medical Writing and Regulatory Affairs

Offices

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