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CRO & Biopharmaceutical Services | Parexel Solutions Biotech Therapeutic Expertise Insights Participate Sites About Newsroom Academy Careers 中国 日本 Contact UsNewsroom Academy Careers 中国 日本 Contact Us Solutions Biotech Therapeutic Expertise Insights Participate Sites AboutSolutions Explore end-to-end solutions throughout development — from portfolio optimization and regulatory strategy, to Phase I-IV clinical trials, market access planning, and more. See solutions WHAT WE DO Portfolio management and asset valuation Early development and innovation Integrated clinical development Approval and access Value substantiation lifecycle management HOW WE DO IT Delivery models Operational excellence Portfolio Management and Asset Valuation Building patient insights into assets, profile and claims Portfolio Optimization Asset Valuation and Indication Prioritization Early Evidence Review Model-Based Drug Development Integrated Development Strategy and Planning Early Development and Innovation Phase I Clinical Trials Proof of Concept Studies: Phase IB-IIA Patient Engagement Strategy and Enrollment Solutions Patient Inclusion Site Alliance Network and KOL Engagement Protocol Optimization Regulatory Strategy Market Access Strategy and Delivery Biomarker and Genomic Medicine Strategy Clinical Trial Supply & Logistics Medical Communications Integrated Clinical Development Phase IIB-IV Clinical Trials Real World Evidence Patient Engagement Strategy and Enrollment Solutions Patient Inclusion Protocol-Driven, Customized Site Solution Strategy Regulatory Strategy, Submissions, Compliance, and Outsourcing Market Access Strategy and Delivery Clinical Development Technology Optimization Clinical Trial Supply & Logistics Medical Communications Approval and Access Real World Evidence Global Regulatory Submissions and Outsourcing Compliance and Risk Management Market Access Strategy and Delivery Medical Communications Value Substantiation Lifecycle Management Real-World Evidence, Market Access Strategy and Planning Regulatory Compliance, Drug Safety and Pharmacovigilance Lifecycle Optimization Medical Communications FSP Delivery Models in Clinical Trials Gain an advantage through FSP Operational Excellence Leveraging AI and digital in clinical development Biotech Clinical Trial SolutionsBiotech Parexel Biotech provides the end-to-end capabilities you’ll need to succeed. We’re fast, flexible, and dedicated to impacting patient lives. Learn moreTherapeutic Expertise Utilize our expertise across therapeutic areas, combining innovative trial designs, leading clinical and regulatory expertise, global reach, and a passion for changing patient lives. See expertise Therapeutic Expertise Neuroscience General medicine Infectious disease & vaccines Inflammation & immunology Oncology Cross-Therapeutic Expertise Cell & gene therapies Pediatrics Rare diseasesInsights Our experts help you stay at the forefront of the industry - and ahead of change. See insights New Medicines, Novel Insights Advancing rare disease drug development Accelerating development of cell and gene therapies Achieving patient-guided drug development Discussions on Diversity Overview Chapter 1 Bridging the Gap Chapter 2 Beyond the Binary The Regulatory Navigator BIOSECURE Act: Implications for US-based drug developers Exploring ICH Q5A revision 2 Potency assurance for CGT products: FDA’s new draft guidance Latest Report New Medicines, Novel Insights: Achieving patient-guided drug development Learn moreParticipate 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. Learn more INTERESTED IN PARTICIPATING? Healthy Volunteers Patient Volunteers Patient Advocacy Groups HEAR FROM REAL PATIENTS Patient Stories TRIAL SITES Baltimore Los Angeles London BerlinSites Want to collaborate with us to offer clinical trials at your site? We would welcome the opportunity to discuss. Learn moreAbout 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. About Parexel Management team Global reach Our DE&I strategy Our ESG strategy Compliance, Tax & Privacy Meet us at an event Management Team Jamie Macdonald Peyton Howell Greg Rush John Bell Michael Crowley Jonathan Shough Sheri McCoy Eric Liu Bill Chase Maykin Ho Michael Bruun John Groetelaars Susan Salka Global Reach Our DE&I Strategy Our ESG Strategy Compliance, Tax & Privacy Compliance & Ethics Tax Strategy Privacy Policy Supplier Data Privacy Requirements Terms of Use French Gender Pay Data UK Gender Pay Data UK Modern Slavery Act Statement EU-U.S. Data Privacy Framework (EU-U.S. DPF) Supplier Diversity Policy Meet us at an Event World Vaccine Congress Patients as Partners U.S. MAPS Americas ASCPT 2024 Annual Meeting ACRP 2024 Managing Complexity in Cell and Gene Trials: Establishing an RBQM Strategy that Drives Better Performance EDI in clinical research: The case for adaptive strategies at every step 17th ISCR ANNUAL CONFERENCE 2024 IncluDE Site Solutions Summit AAN Annual Meeting ASGCT Annual Meeting Dermatology Drug Development Summit EU World Orphan Drug Congress US ISPOR US AIRIS ATS 2024 AACR Annual Meeting BIO International Convention DIA Global Annual Meeting International Society for Cell & Gene Therapy ASCO Final countdown: How to transition your trials under EU-CTR SCRS: Oncology Site Solutions Summit Accelerating Vaccine Development Through Operational Excellence Alzheimer’s Disease vs Multiple Sclerosis Drug Development: Similarities, Differences & New Perspectives Patients as Partners EU Best of ASCO World Drug Safety Congress US World Drug Safety Congress EU PAGE SCRS West Clinical Tech & Innovation Site Solutions Summit PCMG Assembly 2024What can we help you find today? Home Click or scroll The perspectives and opinions expressed in this material represent those of the patient advocate only and should not be considered a solicitation, promotion or advertisement for any services of Parexel, or any drugs or therapies, including those under development. Participating in clinical trials for investigational medicines offers patients potential benefits, such as access to cutting-edge treatments and expert medical care, while contributing to medical research. However, risks may include side effects, unpredictable outcomes, and time commitment. Careful assessment of these factors helps patients make informed decisions. The content of this material, including graphics, images and text, is provided for informational purposes only and does not constitute medical advice, diagnosis or treatment. Please consult your healthcare professional for medical advice. The patient advocate has provided their consent for the use and distribution of this content. Close Patient Story Rare Diseases Oncology Inflammation & Immunology Cell & Gene Therapy Neuroscience When Austin was 3 years old, his parents realized something was wrong. Disclaimer DMD weakens the muscles until the patient can’t walk and greatly shortens their lifespan. There’s no cure. After multiple falls, concussions, and a broken arm, they discovered he had Duchenne muscular dystrophy, a condition diagnosed in 20,000 children globally each year. Now she was the one in need of care — joining the 3.8 million women in the US and many other around the world impacted by breast cancer.Through clinical trials, however, Austin found treatment to slow the disease and live a better life. Today, he’s a college student, co-founder of the nonprofit One Rare, and a member of our Patient Advisory Council — helping us better meet the needs of rare disease patients. Lives can change when you design rare disease trials with care and precision. 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