Our Platform
Sponsors/CROs
Clinical Trial Execution: Important, Complex Problem
For clinical trials that do complete, there is a high degree of post-market failures due to relevance and applicability in real-world settings.
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Today 50% of new treatments fail due to non drug efficacy-related reasons.
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86% of clinical trial sites do not meet enrollment goals.
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Accelerating Trial Success in Real-World, Diverse Communities
Best-in-class operational delivery across indications, trial stages, and study structures through community-based clinicians who know their patients.
Accelerating Trial Execution
Macro delivers consistent, high-performing site operations in ophthalmology, dermatology, and pulmonology. Our embedded coordinators, experienced investigators, and centralized oversight create a site network that activates quickly, enrolls reliably, and generates high-quality data across study phases and designs.
What Sets Macro Apart
Deep expertise in high value therapeutic areas
Our investigators have extensive experience in ophthalmic, pulmonary, and dermatologic studies, including complex biologics and interventional protocols.
Fast activation and disciplined operational delivery
Our centralized contracting, regulatory, and logistics model shortens startup timelines and ensures every site begins study activity with the right staff, equipment, and workflows in place.
Reliable enrollment and strong retention
Macro’s coordinators and community-based clinicians reach patients often missed by traditional centers and support retention through hands on logistics and communication.
Access to diverse real-world populations
We support inclusion of underrepresented patients, improving representation and strengthening generalizability of study outcomes.
End-to-end site support that removes burden from investigators
Macro manages budgeting, contracting, procurement, IRB coordination, staffing, scheduling, and site level logistics.
Study ready infrastructure that produces consistent, high-quality data
Central oversight, trained coordinators, and standardized processes enable clean documentation and strong protocol compliance.
Quality and Compliance
Macro maintains rigorous quality standards that ensure data integrity and reduce risk for sponsors.
- Standardized SOPs and coordinator training
- Centralized quality oversight and real time study monitoring
- Routine data review to identify and resolve issues early
- Structured compliance processes that support clean audits
- Close collaboration with sponsors on reporting and documentation
This disciplined foundation is designed to minimize deviations and maintain the highest standard of trial execution.
Diversity and Community Engagement
Macro’s network is rooted in community-based practices that reflect the demographic and clinical diversity of real-world populations.
We expand access to research by:
- Partnering with clinicians who serve broad and varied communities
- Embedding multilingual coordinators
- Offering travel and logistical support when needed
- Providing free study related evaluations and medications
This approach enhances patient inclusion and improves representativeness in clinical trials.
Proven Track Record
Macro delivers consistent operational performance across ophthalmology, dermatology, and pulmonology. Our sites activate quickly, enroll reliably, and maintain strong protocol discipline through experienced investigators and embedded coordinators.
Sponsors trust Macro for:
- Fast and predictable study startup
- Reliable enrollment across diverse patient populations
- High quality data supported by centralized oversight
- Strong retention driven by community-based clinicians
Macro sites have demonstrated consistent enrollment success, clean data, and broad patient representation.
Therapeutic Areas
Macro conducts therapeutic studies across ophthalmology, dermatology, and pulmonology, supported by experienced investigators and embedded coordinators across CA, WA, NV, TX, New England, and the Tri State region.
Become a Sponsor
Let's Partner On Your Next Trial
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