hyperCORE International

CROs

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For CROs

The Challenges:

Clinical development continues to become more complex. CROs face increasing pressure to identify experienced sites, accelerate study startup, meet aggressive enrollment timelines, and deliver consistent execution across multiple locations. Managing numerous individual site relationships can slow timelines. Today’s studies require strategic partners that can adapt, scale, and consistently deliver.

Benefits:

Partnering with hyperCORE provides streamlined access to a growing network of exceptional clinical research organizations through one strategic relationship.

  • Unified Access: A single strategic partnership provides streamlined access to multiple high-performing clinical research organizations.
  • Speed: Rapid feasibility responses and site identification through one point of contact, with 48–72-hour feasibility turnaround.
  • Expanded Reach: Scale your studies through broader geographic coverage and access to diverse patient populations across the United States.
  • Therapeutic Expertise: Access experienced investigators and proven research sites spanning a broad range of therapeutic areas and study phases.
  • Scalable Solutions: Whether you need a single site or a multi-site strategy, our network supports Phase I–IV clinical trials with the flexibility to scale alongside your program.
  • Strategic Partnership: Build a long-term relationship with a trusted partner that understands your goals, proactively supports your pipeline, and grows with your development needs.

How We Work:

hyperCORE serves as an extension of your study team. We work closely with CROs to understand protocol requirements, identify the most appropriate research organizations, and coordinate feasibility. While hyperCORE manages the partnership and strategy, our partner organizations execute the study, creating a seamless experience from feasibility through study completion.

Our model is designed to be more than transactional. Whether you need support identifying specialized investigators, expanding into new patient populations, responding to an urgent bid defense request, or strengthening site coverage across a therapeutic area, our team is here to help.

Site Models:

  • Practice-Embedded Research Sites: Integrated directly within physician practices, providing immediate access to established patient populations.
  • Integrated Research Sites: Operating in close collaboration with healthcare systems and specialty practices.
  • Dedicated Research Sites: Independent clinical research centers with experienced research teams.

As a vast network of experts in our field, we believe coming together is the key to accelerating research.

hyperCORE International offers the ability to conduct research across all therapeutic areas, providing a vast network of leading clinical research sites committed to the highest standard of excellence in enrollment, data integrity, and timelines. Our network features over 70 research site locations across North and South America, multiple hospital affiliations, remote and mobile units, and expertise in device and therapeutics of all phases of research.  Our partner sites have special expertise and key opinion leaders in endocrine and metabolic studies inclusive of MASH and have on-site FibroScan® machines in many of our locations. They are leading industry representatives in vaccine research including the Clinical Trial Site of the Year for Vaccine Research. Our network also offers broad dermatology expertise with access to more than 1 million patient lives and various medical indications to offer research as a pathway to clinical care.

Our ability to move beyond the constraints and challenges is reflected in our robust clinical trial experience. Our patients are exceptionally diverse in health status, age, race, ethnicity, sex, and co-morbidities. We have enabled our sites to scale quickly to accommodate large volume trials by using shared resources and platforms resulting in rapid study start-up delivery and execution. With hyperCORE’s collaborative approach to clinical research partnership, research has never been more streamlined.

Therapeutic Areas
Cannabis & Psychedelics
Cardiology
COVID- 19 Capabilities
Dermatology Capabilities
Devices / Diagnostics
Endocrinology
Gastroenterology
Gerontology
Gynecology
Hematology
NASH Capabilities
Immunology
Men’s Health
Nephrology
Neurology
Nutrition
Oncology
Ophthalmology
Pain Management
Pediatrics
Podiatry
Psychiatry
Pulmonology
Rheumatology
Smoking Cessation
Urology
Vaccine Capabilities

Phase 1 Details

7 domiciling-capable sites across 5 U.S. states with 18 Principal Investigators

Collectively we have conducted 125 early phase trials — 30 were first-in human trials

60 beds combined

Facilities range from 4,000 to 17,000 SF

Phase 1 Testing / Equipment