- Trusted by 5,000+ people
Be part of something Join a clinical trial near you.
You’ll receive free, study-related medical care from trusted physicians—plus compensation for your time. Clinical trials at Avita are safe, compassionate, and designed with you in mind.
- Trusted by 25+ Sponsors
Your trusted partner for scalable, high-performing clinical research.
We deliver what sponsors and CROs need most—fast startup timelines, reliable patient recruitment, and expert operational support across every study phase.
- Multi-site capabilities
- Data-driven performance
- IRB & FDA Regulated
- Fast trial startup
- IRB & FDA regulated
- Sponsor-centric support
- Participant diversity
Trusted by leaders in global research
Why top sponsors, patients, and partners choose Avita
We’re not just a clinical research company — we’re your growth partner, your compliance ally, and your gateway to smarter, faster studies. Here’s what makes Avita Clinical Research the preferred choice for leading sponsors, diverse patient communities, and a growing network of affiliates.
- Fast trial startup
- Diverse patient recruitment
- Nationwide site network
- Sponsor-first approach
- Real-time reporting
- Regulatory compliance
Experienced medical leadership
Our sites are led by licensed physicians and experienced principal investigators who ensure clinical integrity and patient safety.
Fast trial startup
We help you move from feasibility to first-patient-in with speed and precision — without sacrificing quality or compliance.
Sponsor-first collaboration
We customize processes around your protocol, metrics, and goals — and act as an extension of your research team.
Expanding site network
With dedicated and affiliate sites across multiple states, we help you reach the right participants faster without any hassle.
Transparent reporting
Access real-time insights, enrollment stats, and compliance metrics — so you’re never in the dark about your trial’s progress.
Diversity + innovation
We prioritize representative populations and use technology to improve engagement, data quality, and retention.
Ready to see how Avita can support your research or care journey?
Join a clinical study that makes a difference, for you and for others.
Take an active role in advancing medicine while receiving expert care, access to cutting-edge treatments, and the opportunity to help shape the future of healthcare.
At Avita Clinical Research, we believe that every participant plays a vital role in moving medicine forward. Whether you’re living with a specific condition or simply want to contribute to breakthrough research, we’re here to guide you every step of the way.
Our studies are overseen by licensed physicians, follow strict ethical standards, and offer care at no cost to you. You’ll receive close monitoring, trial-related medical attention, and support from our compassionate clinical team throughout the process.
Participating is always voluntary, safe, and confidential — and you can stop at any time.
Real people. Real care. Real impact.
Here’s how it works — simple, safe, and all about you
Joining a clinical study is easier than you think. We’re here to guide you through each step with care, transparency, and support from day one.
01
Find a study that fits you
We’ll help you explore open trials that match your health history, condition, or goals. Every study is explained in plain language so you feel informed from the start.
02
Talk with our team
If you’re eligible, you’ll speak with our medical team — not a chatbot. They’ll answer your questions, explain next steps, and make sure you’re fully comfortable moving forward.
03
Get free trial-related care
Once enrolled, you’ll receive medical checkups, lab work, or treatment — all related to the study — at no cost. We monitor your safety and progress every step of the way.
04
Help advance medicine for tomorrow
Your participation helps researchers discover better treatments, improve care, and impact future lives. You’re not just joining a study — you’re shaping the future of health.
Partner with Avita for smarter, faster, high-impact trials
From global sponsors to innovative biotech firms, organizations choose Avita Clinical Research for our operational excellence, diverse patient access, and transparent trial execution.
Smarter trials. Stronger partnerships. Proven performance.
Rapid site startup and regulatory alignment
IRB, feasibility, contracting — we move fast and stay compliant at every step. Our experienced startup team minimizes cycle times while ensuring every document, process, and activation is handled with precision and transparency.
Diverse and engaged patient populations
Community-based outreach strategies drive enrollment across age, ethnicity, and socioeconomic backgrounds. We work with local providers and cultural liaisons to ensure patients feel seen, understood, and motivated to participate.
Full transparency from feasibility to close-out
Real-time dashboards, enrollment metrics, visit compliance, and AE reporting — all built into your sponsor view. No hidden delays, no surprise deviations — just clear, consistent data at every milestone.
Sponsor-centric workflows and integration
We adapt to your SOPs, timelines, and systems — whether that means EDC access, integration with your CTMS, or aligning with your monitoring cadence. You stay in control while we drive execution.
Strategic services that support every phase of research and growth
Whether you’re launching a new study, expanding your site capabilities, or refining your patient recruitment strategy — Avita Clinical Research delivers tailored services designed to reduce delays, maximize performance, and build lasting trial success. Explore how our vertically integrated services align with your goals.
Clinical Trial Operations
Launching and managing a clinical trial can be complex — but with Avita, it doesn’t have to be. Our experienced operations team guides you through every phase, from feasibility to close-out, ensuring protocol compliance, coordinated visits, and seamless execution across sites. Whether you’re running a single study or scaling across locations, you’ll get the support and precision needed to accelerate your timeline without sacrificing quality.
Patient Recruitment & Engagement
Finding the right participants shouldn't be a bottleneck. Our patient recruitment strategies combine digital outreach, local community engagement, and culturally sensitive messaging to reach diverse populations that reflect the real world. We not only help you recruit qualified patients faster — we help you keep them engaged through every stage of the study.
Regulatory & IRB Consulting
Delays in IRB approval and documentation can stall even the most promising studies. That’s why we offer tailored regulatory consulting to help you navigate ethics submissions, protocol development, and Good Clinical Practice (GCP) alignment with confidence. Whether you're managing a new trial or adapting mid-study, we keep you compliant, audit-ready, and moving forward.
Data Transparency & Reporting
IRB, feasibility, contracting — we move fast and stay compliant at every step. Our experienced startup team minimizes cycle times while ensuring every document, process, and activation is handled with precision and transparency.
Research Site Network & Affiliations
When you join Avita’s research site network, you become part of something bigger. We support new and established research teams with structured onboarding, hands-on mentorship, and access to an active pipeline of sponsor opportunities. From SOP templates to operational guidance, everything we offer is designed to help your site grow efficiently, compliantly, and with confidence.
Clinical Research Consulting
Whether you’re launching your first study or scaling operations across multiple sites, our consulting team helps you build a stronger research foundation. We offer expert support in SOP development, team structuring, technology adoption, and site readiness. With Avita as your strategic advisor, you’ll avoid costly missteps and stay focused on long-term success.
Site enablement. Strategic consulting. Digital readiness. ↘
Affiliate Partnerships
Becoming a clinical research site doesn’t have to be overwhelming. At Avita, we help new and independent sites step into the world of clinical trials with operational support, sponsor access, and a collaborative network designed to grow with you. From onboarding to patient referrals and trial matching, we make sure you’re ready to run efficient, compliant, and meaningful studies.
- Onboarding & trial readiness setup
- Access to sponsors and CROs
- Templates for SOPs, consent, and contracts
- Patient referrals through our recruitment team
- Ongoing mentorship and study placement
Clinical Research Consulting
Whether you’re launching your first trial or managing multiple sites, our clinical consulting services help you scale with clarity and compliance. We support you through feasibility planning, SOP development, staff training, and regulatory navigation — so you can operate with confidence and credibility.
- Full-site SOP & GCP guidance
- Feasibility and protocol support
- Regulatory + IRB submission help
- Study operations optimization
- Team training and operational workflow setup
Website Development
Your digital presence matters more than ever. We build fast, responsive, and compliant websites for research sites, designed to attract patients, showcase studies, and communicate trust to sponsors. Whether you need a landing page or a full multi-study portal, we design with intention, speed, and compliance in mind.
- Custom site design for clinical research
- Study pages and lead capture integration
- Mobile + HIPAA-compliant builds
- WordPress or custom frameworks
- SEO optimization for local & sponsor visibility
Social Media Marketing
We help research sites and clinical brands reach the right audience with impactful, compliant social media strategies. From patient recruitment to brand-building, our team creates and manages content across Facebook, Instagram, LinkedIn, and more — tailored to engage real people in your community and build long-term visibility.
- Social campaigns for patient recruitment
