Meet Paradigm Clinical Research at SCOPE 2026
Learn how Paradigm’s purpose-built, multi-location research sites expand access, accelerate timelines, and deliver high-quality Phase I–IV clinical trials. Request a meeting with Paradigm’s experts to explore how we can support your upcoming studies.
17th Annual Summit for Clinical Ops Executives (SCOPE)
- Rosen Shingle Creek | Orlando, Florida
- Visit us at Booth 1429 Stop by booth 1429 to meet our team and discuss how we can partner on your next program.
- Schedule a Meeting Request a meeting with our experts using the form on this page.
Your Trusted Clinical Research Site Partner
Conducting patient and healthy volunteer studies with the right clinical research site partner shortens timelines and reduces operational risk. Meet with our leadership and clinical operations team at the 17th Annual Summit for Clinical Ops Executives (SCOPE) to discuss how Paradigm’s multisite integrated approach helps sponsors and CROs:
- Accelerate timelines: streamlined contracting, centralized operations, and fast regulatory turnaround.
- Expand access and diversity: purpose-built sites located in underserved markets to reach underrepresented participants, along with experienced partner principal investigators.
- Increase participation and retention: high engagement, low dropout, and reliable enrollment projections tailored to advance patient-focused clinical trials.
- Deliver high-quality data: experienced investigators, centralized oversight, and operational standardization.
By prioritizing patients and addressing their needs, we strive to make a meaningful impact on advancing medicine and improving patient outcomes.
What Sets Paradigm Apart
- 16+ years conducting full-service Phase I–IV trials
- 6 purpose-built, wholly owned sites Across California, Colorado, and Idaho. Local presence with centralized support.
- 98% participant satisfaction Exceptionally low loss-to-follow-up.
- 6 core therapeutic areas Where we have extensive experience and established multi-site expertise.
Experience the Paradigm Difference & Ensure Your Trial’s Success
- Integrated Site Model We own and operate our sites (not a manager of third-party sites), delivering consistency and accountability across locations.
- Centralized Operations Single point of contact for feasibility, contracting, regulatory, recruitment, and reporting.
- Scalable Recruitment Local PI relationships, EMR access, and centralized recruitment teams to hit timelines.
- Specialized Expertise Therapeutic experience in respiratory, infectious disease & vaccines, dermatology, neurology, endocrine/diabetes, and more.
- Regulatory & Start-up Speed Proven processes that compress budget/contract and regulatory timelines.
Let's Connect at SCOPE — Request a Meeting
Complete the form below, and a member of the Paradigm team will reach out to schedule your meeting during SCOPE.
Because the Future of Medicine
Matters More Than Ever
Paradigm Clinical Research works with all the industry’s leading sponsors and CROs, and we are recognized for our collaborative approach. Our top priorities are open communication, transparency, and partnership, which help us build strong relationships driving successful outcomes for all parties involved.
When you partner with Paradigm Clinical Research, you gain access to a world-class team of clinical research experts who are dedicated to advancing medicine and improving patient outcomes. When high quality clinical trial outcomes depend on reliable patient engagement, investigator and research staff expertise, and accurate data delivery, Paradigm Clinical Research is your partner of choice.