About Us
On the forefront of getting cures to market, there is PPD. We bring the highest caliber of scientific and clinical expertise and quality and speed to the development of the drugs that address the world’s most challenging health concerns.
PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 48 countries and more than 20,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to help clients and partners bend the cost and time curve of drug development and optimize value in delivering life-changing therapies to improve health.

Our clinical monitoring department defines and develops clinical programs. We ensure the highest-quality review of data and effective interaction with study sites, including on-site monitoring throughout a study. Our clinical research associates (CRAs), remote site monitors (RSMs), project assistants (PAs), and client-dedicated teams oversee and administer the health and efficacy of treatments during trials. We support the logistics and organization of clinical sites — ensuring that patients receive needed care, as well as identifying and treating clinical trial participants.

We are passionate about being data and technically agile, driving enhanced value for our clients and patients. Determined to improve patient health, we help PPD provide industry-leading statistical, programming and clinical pharmacology contributions through global delivery, consistent quality adherence and scientific insight. Through a procedural framework based on robust planning and specifications, we work to deliver the highest-quality deliverables — from planning clinical trials and development programs through knowing the results of a study and leading the regulatory submissions.

Are you a data and a people person? Here’s your team. We manage and clean the data collected in a clinical trial — from the design and build of the database and edit checks, through the entry and cleaning of data to the final delivery of clinical trial data. We work closely with the project teams and clients to identify best practices and processes, meet and exceed our clients’ needs, and do the right thing to earn their trust.

If you’re a strategic thinker, planner and multitasker as comfortable working independently as you are on a team in delivering compliant deliverables based on solid judgment, PPD is the place to be. Our 775+ regulatory experts in 29 countries contribute the regulatory strategy and knowledge to help our clients navigate the challenging regulatory environment — and help get life-changing therapies to patients faster. With our end-to-end solutions, we work to ensure regulatory compliance throughout the product life cycle, while helping to advance global product development.

Our detailed, goal-oriented team members manage the safety profile of new drugs in clinical trials, oversee case-processing activities through all phases of development and perform regulatory reporting and medical monitoring tasks.

If you think improving health is important, then think of joining PPD. If you want to be proud of what you do, be with PPD. Our colleagues in corporate strive for excellence in every task, at every moment. We are game changers seeking improvements to processes and more efficient ways of working or adapting to changing financial and industry environments.

Your Potential with PPD
PPD Brings Life-changing Therapies to Market