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CRO & Biopharmaceutical Services | Parexel SolutionsBiotechTherapeutic ExpertiseInsightsParticipateSitesAbout Search Newsroom Academy Careers 中国 日本 Contact Us Main Menu Newsroom Academy Careers 中国 日本 Contact Us SolutionsBiotechTherapeutic ExpertiseInsightsParticipateSitesAbout Close Menu Solutions 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 Medical affairs Portfolio management and asset valuationBuilding patient insights into assets, profile and claimsPortfolio optimizationAsset valuation and indication prioritizationEarly evidence reviewModel-based drug developmentIntegrated development strategy and planningEarly development and innovationPhase I Clinical TrialsProof of Concept Studies: Phase IB-IIAPatient Engagement Strategy and Enrollment SolutionsPatient InclusionSite Alliance Network and KOL EngagementProtocol OptimizationRegulatory StrategyMarket Access Strategy and DeliveryBiomarker and Genomic Medicine StrategyClinical Trial Supply & LogisticsMedical CommunicationsIntegrated clinical developmentPhase IIB-IV Clinical TrialsReal World EvidenceOperationalize post-trial access with a proven platform approachPatient Engagement Strategy and Enrollment SolutionsPatient InclusionProtocol-Driven, Customized Site Solution StrategyRegulatory Strategy, Submissions, Compliance, and OutsourcingMarket Access Strategy and DeliveryClinical Development Technology OptimizationClinical Trial Supply & LogisticsMedical CommunicationsApproval and accessReal World EvidenceGlobal Regulatory Submissions and OutsourcingCompliance and Risk ManagementMarket Access Strategy and DeliveryMedical CommunicationsValue substantiation lifecycle managementReal-World Evidence, Market Access Strategy and PlanningRegulatory Compliance, Drug Safety and PharmacovigilanceLifecycle OptimizationMedical CommunicationsFSP delivery models in clinical trialsGain an advantage through FSPOperational excellenceLeveraging AI and digital in clinical development Close Menu Biotech Parexel Biotech provides the end-to-end capabilities you’ll need to succeed. We're fast, flexible, and dedicated to impacting patient lives. Learn more Close Menu Therapeutic 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 diseases Close Menu Insights Our experts help you stay at the forefront of the industry - and ahead of change. See insights New Medicines, Novel Insights Advancing precision oncology 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 Gene therapy: are high costs and manufacturing complexities impeding progress? New FDA draft guidance: Implications for simplifying interchangeability for biosimilars in the US Key implications for nonclinical development: FDA guidance on human gene therapy products incorporating human genome editing Latest Report New Medicines, Novel Insights: Advancing precision oncology Learn more Close Menu Participate 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 Berlin Close Menu Sites Want to collaborate with us to offer clinical trials at your site? We would welcome the opportunity to discuss. Learn more Close Menu About 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 Leadership team Global reach Our DE&I strategy Our ESG strategy Compliance, tax & privacy Meet us at an event Leadership teamBoard of DirectorsGlobal reachOur DE&I strategyOur ESG strategyCompliance, tax & privacyCompliance & EthicsTax StrategyPrivacy PolicyCookies and other web trackingSupplier Data Privacy RequirementsTerms of UseFrench Gender Pay DataUK Gender Pay DataUK Modern Slavery Act StatementData Privacy FrameworkSupplier Diversity PolicyMeet us at an event Close Search What 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 Oncology Rare Diseases Inflammation & Immunology Cell & Gene Therapy Neuroscience Sara's only symptom was fatigue. But after some routine tests, she was diagnosed with breast cancer. Pause Background Motion Disclaimer Now she was the one in need of care — joining the 3.8 million women in the US and many others around the world impacted by breast cancer. For years she'd worked at a hospital, onboarding new doctors and making care possible for others. She started radiation. A new, promising chemotherapy treatment was also available, so she joined the clinical trial. That decision changed her life. Today, she’s cancer free — and works at Parexel to help ensure our trial sites are prepared to meet the needs of patients like her. Lives can change when you design oncology trials with speed and precision. Utilize the right experts, with the right specialization Find the patients you need and earn their trust Satisfy global regulations to get your treatment to patients safely and quickly Design studies and endpoints with market access in mind What we do, we do Our Experts Our oncology specialists collaborate to help get your treatment to patients like Sara faster. MORE EXPERTS Edina Tolnay, M.D., Ph.D. Global TA Section He... Sinan Sarac, M.D., Ph.D., M.Sc. Senior Vice Presiden... Claudia Marques Vasconcelos Global TA Section He... Floris Höppener, M.D. Global TA Section He... Gamal ElSawah, M.D. Global TA Section He... Maria Cristina Villarroel Global TA Section He... Close Our Experts Gwyn Bebb, M.D., BM, BCh, Ph.D. Senior Vice President, Global Therapeutic Area Head – Oncology Gwyn is a licensed medical oncologist with more than 20 years’ experience in academia and the clinical research and biotechnology industries. At Parexel, he leads the research and development of new cancer treatments for biopharmaceutical customers worldwide. His depth of expertise in oncology drug development and proven experience in leading cross-functional teams positions him as an invaluable resource for customers and a natural leader of our global oncology franchise. Our oncology team is 1,000+ strong, with experience across the oncology continuum, to match the needs of your trial. Advanced modeling and simulation allow us to predict drug effects in advance , saving time, money, and resources. Our experience with oncology clinical trial sites around the world allows us to accelerate study start-up. North America South America Europe APAC Middle East & Africa Our application of real-world data allows us to find the right study participants fast. Our global regulatory team keeps everything running smoothly. And our patient-first approach results in deeper, more relevant insights for trial design and execution. TACTICS BENEFITS MAY INCLUDE What can we do to help you change patient lives? See oncology capabilities Explore oncology careers Contact us Discover other patient stories Rare Diseases When Austin was 3 years old, his parents realized something was wrong. Multiple falls, concussions, and a broken arm led to a diagnosis. View story I&I Tina had lost her father to Crohn's disease. Now she faced her own diagnosis — and it derailed her life. View story Cell & Gene Therapy One night, while watching TV with her husband, Robyn felt a lump in her neck. As a doctor, she knew the risk. View story Neuroscience While running a triathlon, Andrea stumbled and realized something was wrong. She thought it was just an injury. But it was much more. View story 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 We focus on patients, because they inspire us to deliver better trials, faster than ever. So we can make a difference for more patients like Sara. Disclaimer Who we are, Parexel is proudly among the world’s largest clinical research organizations A dedicated CRO providing the full range of Phase I to IV clinical development services and leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals works in partnership with biopharmaceutical leaders and sites to design and deliver clinical trials with patients in mind, to make clinical research a care option for anyone, anywhere. Contact us Meet us at an event Resources My Communication Preferences Invoicing PO Terms and Conditions Regional Websites Japan China Quick Links Participate Sites Careers Newsroom Academy 2520 Meridian Parkway, Durham, NC 27713 +1 919 544 3170 Privacy Policy Cookies Terms of Service Modern Slavery Statement Act © 2024. Parexel International (MA) Corporation. All Rights Reserved.
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