Early Phase Clinical Trials
Multi-disciplinary early phase approach accelerating proof of concept
Service · OtherCompany source
Company profile
About Parexel
Parexel is a leading global contract research organization (CRO) that provides comprehensive biopharmaceutical services spanning the entire drug development lifecycle. The company delivers end-to-end solutions from portfolio optimization and early phase clinical trials through Phase I-IV studies, regulatory submissions, market access planning, and post-approval lifecycle management. Parexel combines operational expertise with its proprietary ParexelAI technology suite to accelerate clinical development with greater speed, quality, and efficiency. The company specializes in multiple therapeutic areas including oncology, neuroscience, immunology, infectious diseases, hematology, ophthalmology, and rare diseases. Parexel's services encompass clinical trial management, regulatory strategy and submissions, real-world evidence generation, pharmacovigilance, medical communications, and market access consulting. With a team that includes more than 80 former regulatory agency professionals and access to nearly 2,500 clinical trial sites globally, Parexel serves pharmaceutical companies, biotech firms, and medical device manufacturers. The company offers flexible delivery models including functional service provider (FSP) arrangements and customized site solutions. Parexel's integrated approach combines clinical, regulatory, and market access expertise to optimize development strategies, accelerate patient enrollment, ensure regulatory compliance, and maximize the commercial potential of new therapies throughout their lifecycle.
Company description Parexel official website
Primary marketClinical Trials & Research
Commercial modelCommercial information available on request
Company presenceOfficial website
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01 · Operating footprint
Where the Company operates
Company-profile context for clinical focus, customers, deployment, integration, milestones, and partnerships.
Clinical focus
- Cell and gene therapies
- General medicine (gastroenterology, respiratory, endocrine/metabolic, cardiovascular, women's health)
- Hematology (lymphoma, AML, MDS, multiple myeloma)
- Immunology (dermatology, allergy)
- Infectious diseases and vaccines
- Neuroscience (neurology, psychiatry)
- Oncology (bladder, breast, colorectal, gynecologic, head and neck, liver, lung, pancreatic, prostate cancer)
- Ophthalmology
- Pediatrics
- Rare diseases
Who it serves
- Biotech firms
- Medical device manufacturers
- Pharmaceutical companies
Deployment & integration
Cloud Saas · Other deployment with recorded integration context.
Geographic context
MarketsGermany (Berlin trial site) · Global · UK (London trial site) · USA (Baltimore, Los Angeles trial sites)
Company sourceOfficial website
Company milestones
Platform expansion
ParexelAI platform launch and integration with Paradigm for AI-enabled clinical development
Partnerships
Recorded partners
- 2,500+ clinical trial sites globally
- Paradigm (mentioned in ParexelAI context)
- Site Alliance Network
02 · Flagship portfolio
Products, workflows, and platform capabilities
Selected source-backed Company products and the available commercial context.
FSP Delivery Models
Functional Service Provider models for clinical trials
Service · OtherCompany source
Global Regulatory Submissions and Outsourcing
Tailored regulatory and market access strategies for global reach
Service · OtherCompany source
ParexelAI
AI-enabled clinical development suite accelerating patient outcomes
Platform · Cloud SaaSCompany source
Phase IIB-IV Clinical Trials
Integrated clinical development with patient-informed protocols
Service · OtherCompany source
Portfolio Management and Asset Valuation
Optimize portfolios with integrated clinical, regulatory, and market access strategies
Service · OtherCompany source
Real-World Evidence
Post-approval studies and lifecycle management services
Service · OtherCompany source
03 · Research intelligence
Research Intelligence evidence
Publications, preprints, clinical validation, and regulatory records in Evidence Position order.
Evidence position
Publications, clinical validation, and regulatory records connected to this Company appear here.
Research
Publications & preprints
Cost-effectiveness of etranacogene dezaparvovec compared to eftrenonacog alfa for the treatment of adult patients with severe and moderately severe haemophilia B in Sweden.Journal of medical economics · Dec 1, 2026
Assessing the consistency of overall survival extrapolations in Swedish health technology assessment reports of oncology treatments using extended follow-up data.Journal of medical economics · Dec 1, 2026
Translational and phase I evaluation of AZD0292, a novel, half-life extended anti-Pseudomonal Psl-PcrV bispecific monoclonal antibody.The Journal of infectious diseases · Oct 9, 2026
Evaluating the Impact of CYP1A2 Inhibition on the Pharmacokinetics of Savolitinib: A Phase 1 Open-Label Study.Pharmacology research & perspectives · Oct 1, 2026
Algorithms to Identify Preeclampsia in Routinely Collected Healthcare Data: A Systematic Review.Pharmacoepidemiology and drug safety · Oct 1, 2026
Risk of drug-induced liver injury in multiple system atrophy patients treated with KM-819 is potentially associated with the HLA-DPB1*05:01:01:01 allele.The pharmacogenomics journal · Sep 28, 2026
Clinical validation
Clinical-trial records
No linked records are currently available.
Regulatory
Regulatory records
No linked records are currently available.
04 · Company-reported outcomes
Outcomes and case studies
Company-reported outcomes and customer stories are distinct from linked Research Intelligence evidence.
Accelerated patient outcomes
Through AI-enabled clinical development suite
Greater speed, quality, and efficiency
ParexelAI delivery capabilities
05 · Leadership
Leadership team
Leadership profiles and professional links from the current Company record.
No active leadership profiles are currently listed.
06 · Company updates
Updates from Parexel
Recent articles published on Parexel's official website.
07 · HAIC coverage
Coverage and analysis
Health AI Central reporting that mentions this Company.
No HAIC coverage is currently linked to this Company.
08 · Official presence
Company sources and channels
Curated official destinations from the active Company record.
09 · Market pathway
Additional Companies in this Market
Other active Companies in the same market, selected alphabetically from the HAIC directory.
Market context
Clinical Trials & Research
Companies using AI to optimize clinical trial design, accelerate patient recruitment, match patients to trials, predict trial outcomes, or improve clinical research efficiency. Includes patient enrollment and screening platforms, AI-powered trial matching, and tools that reduce the time and cost of bringing new treatments to market.
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10 · Pro research
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Expanded Company research is in development.
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Deeper Company research is coming soon.
Pro Research will introduce expanded technical context, linked evidence analysis, and comparative Company research.
Linked research, clinical, and regulatory source pathways.
Expanded product, deployment, integration, and partnership research.
Record-level provenance and review context.