For over 30 years, Parexel has proven to be a trusted partner for the complex development journey required of biopharmaceutical and medical device companies. We’re also an astute guide, able to simplify that journey for our clients, so safe new products can reach patients more quickly.
At the heart of getting medicines to those who need them.
As one of the world’s leading global clinical research organizations (CRO), we provide the clinical development capabilities and integrated consulting expertise it takes to streamline development every step of the way — faster and more cost-effectively. From decentralized clinical trials to regulatory consulting services and leveraging real-world insights, our therapeutic, technical, and functional ability is underpinned by a patient-first culture embedded in our DNA. Our over 18,000 employees have a deep conviction in what we do, and together with our customers, we are shaping the next generation of therapies, one patient at a time.
Specific Areas of Activity
What do we do?
WHAT DO WE DO?
Globally Integrated Science Taking Your Journey to Global Markets
It can be a long and complex journey, taking your scientific innovations out to the world. This is only the first reason why Parexel® is the perfect partner to help you get there. As one of the world’s largest and most experienced biopharmaceutical service providers, we have the global infrastructure, harmonized protocols, and advanced technologies to uncomplicate the process for you, accelerate your time to market and contain your development costs while minimizing risks of late phase failure. It all begins with our end-to-end approach to conducting clinical trials.
From feasibility analysis, site selection and patient recruitment to clinical monitoring, data collection and management on through NDA preparation, submission, and post-approval studies, Parexel is committed to your entire journey.
Whatever the size or scope of your study, Parexel provides the comprehensive clinical research services you need, from First-in-Human through Phase IV and Post-marketing follow-through. We also have the regulatory expertise, clinical trial operations management, payer and market access planning, medical education and communications capabilities to see your journey through efficiently and effectively.
Explore every phase of our clinical services for a complete picture.
Key areas of focus
Auditing – Data Management – Early Clinical Phases – eCRF – Imaging – IMP – Packaging – IMP Storage – Information – IVRS/IWRS -Laboratory – Late phase IV – Logistics – Marketing / Sales – Medical Advising – Medical Devices – Medical Writing – Meeting & Event -Organization – People selection & placement – Pharmacovigilance & Drug – Project Management – Regulatory – Safety – Statistics – Training & coaching – Translation
General Manager Business and Administration