Expand Patient Access. Accelerate Enrollment. Improve Trial Outcomes.
Industry PartnersORSO Health connects your trials to community-based patient populations through a research model designed for speed, quality, and scalability.
Every access bottleneck, solved.
The three things that slow traditional research are the three things the Orso network is built to fix — so you spend less time on logistics and more time enrolling.
Site-by-site contracting for a drug startup delays patient enrollment by months.
The same patient pools hinder recruitment and extend timelines.
Narrow access yields populations that don't reflect real-world patients.
One MSA covers every site — studies go active in under 30 days on average.
A community network attracts new, engaged patients, facilitating enrollment.
Diverse community sites enroll the patients your therapy is designed to serve.
Site-by-site contracting for a drug startup delays patient enrollment by months.
One MSA covers every site — studies go active in under 30 days on average.
The same patient pools hinder recruitment and extend timelines.
One MSA covers every site — studies go active in under 30 days on average.
Narrow access yields populations that don't reflect real-world patients.
Diverse community sites enroll the patients your therapy is designed to serve.
Same study. A wider front door. See how the Orso network works. →
A Model Built for Execution
Our infrastructure is designed to move quickly while maintaining the highest standards of quality and compliance.
- Multi-Specialty Investigator Network
- 100% Community Clinic–Integrated Research Sites
- Rapid Site Activation (4-8 weeks)
- Centralized study startup workflows
- Centralized Quality, Regulatory, and Operational management
- EMR-based pre-screening workflows
- Dedicated recruitment and retention support
Site Readiness
We don’t just place studies.
We build sites that can run them.
Many high-value and historically underrepresented patient populations receive their care in community practices that have never had the infrastructure or resources to participate in clinical trials. Orso identifies these practices and investigators, prepares and trains their teams, and provides the operational, regulatory, quality, and research infrastructure needed to successfully conduct clinical trials.
The result is a scalable, multi-specialty research network embedded directly within community care—giving industry partners access to investigators and patient populations their trials may otherwise never reach, while bringing innovative treatment options closer to where patients already know and trust their physicians.
- Step 01
Identify and recruit
We source community practices with the right patient panels for your therapeutic area — regardless of prior research experience.
- Step 02
Train and credential
Sites receive comprehensive training that goes well beyond GCP and protocol requirements — covering clinical research fundamentals from the ground up.
- Taught by seasoned clinical trialists
- Tailored to every role on the site team
- Orso guides the site through every step of the process
- Step 03
Activate and support
Sites go live with Orso coordinators embedded — ensuring protocol compliance and enrollment momentum from day one.
The result: a broader, more diverse site network — built on physician relationships patients already trust, with the infrastructure to perform.
A SIMPLER WAY TO WORK WITH US
Seamless multi-site activation.
One agreement, multiple sites, coordinated start-up - so you spend less time on contracting and more time enrolling.
One MSA, multiple sites
A single master agreement and budget streamline activation across all sites—eliminating site-by-site contracting.
Start-up in under 2 months / less than 60 days
Coordinated start-up across the network gets your study active in less than 30 days on average.
One MSA, multiple sites
Every site runs on standardized procedures and workflows, so quality and execution stay consistent network-wide.
Built In Experience
Quality and oversight, in-house
Dedicated internal teams safeguard quality, compliance, and enrollment at every stage of your study.
In-house quality & safety team
Continuous monitoring and oversight to protect participant safety and study quality.
In-house regulatory team
Dedicated regulatory expertise to keep submissions, approvals, and compliance on track.
In-house recruitment team
Multi-modality recruitment pathways to reach and enroll the right patients faster.
FAQs
for Physicians Interested in Becoming a Clinical
What is Orso Health?
Orso Health is a community-based clinical research organization that integrates research directly within physician practices and healthcare networks. We partner with investigators and clinics to expand patient access to clinical trials while supporting sponsors with high-quality study execution, operational oversight, and patient-focused recruitment strategies.
What therapeutic areas does Orso Health support?
Orso Health supports studies across multiple therapeutic areas including allergy & immunology, asthma, pulmonology, ENT, dermatology, oncology, and rare diseases. Our network continues to expand through partnerships with specialty and community-based healthcare providers.
What makes Orso Health different from traditional research sites?
Our model is built around integrating research into trusted clinical environments where patients already receive care. This allows us to leverage established physician-patient relationships, access diverse patient populations, improve engagement and retention, and reduce operational barriers often seen with standalone research sites.
How does Orso Health support patient recruitment?
We use a multi-layered recruitment approach that includes physician referrals, EMR-based patient identification, chart reviews, community outreach, digital recruitment campaigns, referral partnerships, and direct engagement with treating providers. Our integrated clinic model allows research opportunities to be introduced during routine patient care visits.
How does Orso Health ensure quality and compliance?
Orso Health maintains centralized operational oversight, standardized SOPs, quality review workflows, regulatory support, and ongoing staff training aligned with ICH-GCP and ALCOA++ principles. We utilize centralized electronic systems for e-Source and e-Regulatory document management to support data integrity and inspection readiness.
Can Orso Health support rapid site activation and expansion?
Yes. Our operational infrastructure is designed to support efficient study startup and scalable site deployment. Through our integrated network model, we can support expansion into multiple community based locations while maintaining centralized oversight and standardized processes.
What types of patient populations can Orso Health access?
Our network supports access to diverse and underserved patient populations across Southern California and Arizona. Because research is embedded within active community clinics, we are able to engage patients who may not traditionally participate in clinical research.
How involved are investigators in study oversight?
Our investigators remain actively engaged in participant safety oversight, eligibility review, protocol compliance, and clinical decision-making. Orso Health provides operational and administrative support that allows investigators to maintain oversight while minimizing disruption to clinical practice workflows.
What operational support does Orso Health provide to sponsors?
We provide comprehensive site support including feasibility assessments, regulatory management, startup coordination, patient recruitment, source documentation, visit coordination, investigational product management, vendor coordination, quality oversight, and sponsor communication management.
How can sponsors engage with Orso Health for upcoming studies?
Sponsors can connect with Orso Health to discuss upcoming protocols, patient population needs, geographic considerations, and study timelines. Our team works collaboratively with sponsors to identify the best-fit investigators and operational strategy to support successful trial execution.
Better representation. Stronger outcomes.
Expanding beyond traditional trial environments allows sponsors to:
- Improve diversity in enrollment
- Generate more representative, real-world data
- Strengthen overall study quality and reliability
