Explore end-to-end solutions throughout development — from portfolio optimization and regulatory strategy, to Phase I-IV clinical trials, market access planning, and more.
Get the personal, responsive, and committed approach of a small CRO, with all the benefits of a large CRO, to help you develop life-changing treatments for patients.
Step into the world of biotech leaders and hear the untold stories behind their journeys to bring breakthrough innovations to life.
Utilize our expertise across therapeutic areas, combining innovative trial designs, leading clinical and regulatory expertise, global reach, and a passion for changing patient lives.
Our experts help you stay at the forefront of the industry — and ahead of change.
Optimizing the clinical research workforce: An industry analysis by Parexel
At the heart of Parexel sits the world’s most unique insight-generation engine: our people.
Thinking about joining a clinical trial? Learn the drug development process, what it’s like to participate, how to find a trial, and answers to frequently asked questions.
Clinical study participation represents a deeply personal decision with potentially far-reaching impact, as evidenced by these inspiring individual stories that highlight both the life-changing potential for participants and the broader advancement of healthcare for all.
Want to collaborate with us to offer clinical trials at your site? We would welcome the opportunity to discuss.
Our Enabling Successful Sites thought leadership series pairs site representatives with clinical operations experts to identify root causes of investigative site challenges and develop collaborative solutions.
We are one of the largest CROs in the world, speeding life-changing medicine to market by engaging patients With Heart™. Learn about who we are, what we do, and what we believe.
Get the personal, responsive, and committed approach of a small CRO, with all the benefits of a large CRO, to help you develop life-changing treatments for patients.
Step into the world of biotech leaders and hear the untold stories behind their journeys to bring breakthrough innovations to life.
Our experts help you stay at the forefront of the industry — and ahead of change.
Optimizing the clinical research workforce: An industry analysis by Parexel
At the heart of Parexel sits the world’s most unique insight-generation engine: our people.
Thinking about joining a clinical trial? Learn the drug development process, what it’s like to participate, how to find a trial, and answers to frequently asked questions.
Clinical study participation represents a deeply personal decision with potentially far-reaching impact, as evidenced by these inspiring individual stories that highlight both the life-changing potential for participants and the broader advancement of healthcare for all.
Want to collaborate with us to offer clinical trials at your site? We would welcome the opportunity to discuss.
Our Enabling Successful Sites thought leadership series pairs site representatives with clinical operations experts to identify root causes of investigative site challenges and develop collaborative solutions.
Webinar
November 26, 2025
Time: 7:00 AM IST (New Delhi) | 9:30 AM CST (Beijing) | 10:30 AM JST (Tokyo) | 10:30 AM KST (Seoul) | 12:30 PM
Leverage Parexel's regional expertise to accelerate your clinical development programs
Date: Wednesday, 26 November 2025
Time: 7:00 AM IST (New Delhi) | 9:30 AM CST (Beijing) | 10:30 AM JST (Tokyo) | 10:30 AM KST (Seoul) | 12:30 PM AEDT (Sydney)
Duration: 70 minutes
Accelerate Your Global Clinical Strategy
Join us for an exclusive webinar where Parexel's regional experts reveal how sponsors can strategically incorporate Australia and Latin America into their global clinical trial portfolio. From Australia's renowned fast-track pathways and generous R&D tax incentives to Latin America's transforming regulatory landscape, this session delivers actionable insights on navigating regulatory pathways, maximizing cost efficiencies, and optimizing patient recruitment across these high-potential regions.
Why Attend:
Drawing on Parexel's extensive regional expertise, our specialists will equip you with concrete strategies to seamlessly integrate these valuable markets into your global clinical development portfolio—delivering faster start-up times, significant cost efficiencies, and enhanced patient recruitment.
Register today to transform your global trial strategy with Parexel's regional expertise.
Featured Speakers:
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Natasha Steyn, Executive Director, Clinical Operations, Parexel International Bringing 20+ years of pharmaceutical industry experience, Natasha oversees clinical operations across multiple regions, applying her extensive background in clinical research, project leadership, and line management to ensure regional excellence. |
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Anita Patel, Senior Director, Regulatory Delivery, Parexel International With over 20 years of regulatory experience across CROs and pharmaceutical industries, Anita leads 165+ professionals throughout the Americas, providing strategic expertise in clinical trial regulation, marketing authorization, and lifecycle management. |
