Phase III clinical trials: Right where you need us
The challenges of conducting and managing the numerous sites, organizations, and data systems of today’s larger, multinational Phase III clinical trials have never been greater. These complex clinical trials require both global clinical resources and robust technology to recruit patients efficiently, initiate sites quickly, and provide cost-effective study management. Selecting the right Clinical Research Organization as your strategic partner for these pivotal trials means finding a company with a broad array of specialized knowledge and infrastructure, including in-depth therapeutic-area expertise, clinical trial experience, global patient and investigator resources, and regulatory knowledge. In addition, your CRO should be able to provide a full range of eClinical technologies – not only the basic eClinical systems such as EDC, CTMS, and RTSM, but also predictive modeling systems for patient recruitment, adaptive trial technology, medical imaging, and global communications systems – technologies that facilitate trial efficiency, cost reductions, and faster development times.
PAREXEL is right where you need us with the global experience, infrastructure, knowledge, and technology to conduct pivotal clinical trials of any size, anywhere in the world. As one of world’s largest Clinical Research Organizations, PAREXEL offers Phase III resources in North and South America, Europe, Africa, and Asia, so we can access a wide selection of sites and diverse patient populations – helping you accelerate trial start-up and lower the cost of your Phase III clinical trial program. We can plan and manage every aspect of your pivotal trials: study design and protocol development; site and patient recruitment; study monitoring, database and document design; clinical logistics; and medical writing.
PAREXEL’s experience conducting thousands of Phase III trials across the full spectrum of therapeutic areas also gives you the advantage of our unsurpassed network of pre-qualified investigators and trial sites. We also have the local resources and knowledge to understand the country-specific regulations, clinical requirements, and cultural differences – giving us the insight to efficiently support your development needs anywhere in the world.
Our proven Phase III clinical services include:
- Complete clinical development services
- Full range of integrated eClinical technologies
- Advanced study start-up and patient recruitment strategies
- Proven site management metrics and best practices
- Access to high-value investigators
- Extensive therapeutic area experience