Search CROs

• Clinical Operations
• Phase I Clinical Trials
• Phase II Clinical Trials

Global CRO delivering clinical trial management, regulatory consultancy, data management, and medical writing for biotech, pharma, and medical device companies across Phase I–IV studies and real-world evidence programs.

• Clinical Operations
• Phase I Clinical Trials
• Phase II Clinical Trials

ObvioHealth delivers decentralized and hybrid clinical trial solutions through its ObvioGo platform, enabling sponsors to simplify study design, boost participant engagement, and accelerate enrollment across 40 countries.

• Clinical Operations
• Clinical Trial Services
• Data Management & eClinical

Curavit is an innovation CRO specializing in decentralized and virtual clinical trials, offering a comprehensive suite of CRO services from study design through FDA submission with a proprietary Virtual Clinical Site platform.

• Clinical Operations
• Phase I Clinical Trials
• Phase II Clinical Trials

Sacura specializes in clinical trial management and regulatory support for biotech and pharma companies, with expertise in complex international studies and late-stage preclinical-to-market development planning.

• Clinical Trial Services
• Regulatory Affairs
• US FDA Regulatory Strategy

Dermatology-focused CRO providing integrated, turnkey solutions across non-clinical, clinical, and regulatory development from concept to commercialization.

• Clinical Operations
• Phase I Clinical Trials
• Phase II Clinical Trials

Specialized CRO focused on metabolic diseases (obesity, diabetes, MASLD/MASH, cardiovascular, chronic kidney disease) with two decades of expertise, a nationwide registry of 180,000+ participants, and full-service clinical development capabilities from Phase 1 through Phase 3.

• Clinical Operations
• Phase I Clinical Trials
• Phase II Clinical Trials

Full-service CRO specializing in oncology clinical trials, from preclinical IND-enabling studies through Phase I–III trial management, with expertise in First-in-Human studies for new cancer therapies.

• Biostatistics & Statistical Programming
• Cardiovascular & Metabolic Specialty Services
• Central Laboratory Services

Clario provides comprehensive clinical trial endpoint solutions spanning cardiac safety, eCOA, medical imaging, respiratory, and precision motion analysis, supporting approximately 70% of FDA and EMA novel drug approvals over the past decade.

• Bioanalysis
• Biostatistics & Statistical Programming
• Central Laboratory Services

Full-service CRO delivering clinical trial management across early to late phases, with specialist expertise in rare diseases and oncology.

• Biostatistics & Statistical Programming
• Clinical Operations
• Phase I Clinical Trials

Full-service CRO delivering clinical trial services across Asia Pacific, with 50+ years of cumulative experience managing Phase I–IV trials and expertise in oncology, cardiovascular, CNS, and infectious disease indications.

• Biostatistics & Statistical Programming
• Clinical Operations
• Data Management & eClinical

Integrated biometrics CRO delivering clinical data management, biostatistics, statistical programming, and medical writing with AI augmentation and GxP validation for biotech sponsors across all phases of clinical development.

• Biostatistics & Statistical Programming
• Clinical Operations
• Phase I Clinical Trials

Full-service CRO providing clinical trial management, regulatory consulting, pharmacovigilance, biostatistics, and medical writing across 40+ countries with AI-secure eClinical systems and patient-centered trial design.

• Biostatistics & Statistical Programming
• Clinical Operations
• Phase I Clinical Trials

Citeline provides clinical trial intelligence, planning, feasibility, patient engagement, and regulatory compliance solutions to pharmaceutical sponsors. The platform delivers benchmarking across 400k+ trials, site selection, protocol optimization, and disclosure management services.

• Biostatistics & Statistical Programming
• Central Laboratory Services
• Clinical Imaging Core Lab

Fortrea is a leading CRO advancing clinical trials through patient-focused clinical solutions that accelerate clinical development and drive trial success.

• Biostatistics & Statistical Programming
• Central Laboratory Services
• Clinical Imaging Core Lab

Full-service CRO specializing in clinical trial management, advanced medical imaging, dosimetry, and data management across oncology, dermatology, and radiopharmaceutical therapies.

• Biostatistics & Statistical Programming
• Clinical Operations
• Phase I Clinical Trials

European full-service CRO supporting clinical development from Phase I to IV and non-interventional studies, with expertise in clinical monitoring, data management, biostatistics, medical writing, and regulatory affairs.

• Biostatistics & Statistical Programming
• Clinical Operations
• Phase I Clinical Trials

YPrime delivers configurable eCOA, IRT, and eConsent clinical trial technology platforms with consulting services, supporting ~1,000 studies globally across 19+ therapeutic areas.

• Bioanalysis
• Biostatistics & Statistical Programming
• Cardiovascular & Metabolic Specialty Services

Global CRO with 26,000+ employees offering integrated clinical development, regulatory affairs, and commercialization services. Helped develop or commercialize 96% of FDA-approved oncology drugs and 93% of EMA-authorized oncology products in the last five years.