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Our Platform

Sponsors/CROs

Accelerate life-saving treatments.

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.

Some of Our Partners

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.

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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.

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community doctor

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.

Ophthalmology

Macro operates one of the most rapidly expanding ophthalmology research networks in the country, powered by retina specialists and comprehensive ophthalmologists.

Where We Excel

  • Reliable enrollment in retina and anterior segment studies
    Strong representation of diverse real-world populations
  • Clean data and low protocol deviations
  • Physician investigators experienced in Phase 2 and Phase 3 trials

Indication Experience

  • Wet AMD
  • Dry AMD
  • Geographic Atrophy
  • Diabetic Retinopathy
  • Diabetic Macular Edema
  • Thyroid Eye Disease
  • Glaucoma

Investigational Product Experience

  • Biologics delivered by infusion, subcutaneous, or intramuscular routes
  • Oral therapies
  • Intravitreal Injections

 

Dermatology

Macro supports community dermatologists engaged in inflammatory, immunologic, and procedural dermatology trials.

Focus Areas

  • Atopic dermatitis
  • Psoriasis
  • Acne and rosacea
  • Urticaria and immunologic skin conditions
  • Injectable therapeutics

Why Sponsors Partner with Macro Dermatology

  • Fast activation at high-volume clinics
  • Predictable enrollment of treatment naive populations
  • Standardized protocols that support clean documentation and adherence

 

Pulmonology

Macro partners with pulmonologists who manage significant populations of respiratory patients across diverse communities.

Focus Areas

  • Asthma
  • COPD
  • Allergic and immunologic airway disease
  • Inhaled, infused, and oral therapies

Why Sponsors Partner with Macro Pulmonology

  • Real-world patient access across multiple regions
  • Strong retention through logistical and communication support
  • Operational consistency across complex multi-visit protocols