Macro Trials
Macro is the partner behind your most reliable clinical trial sites
We collaborate with sponsors and CROs to deliver high-performing, research-experienced investigators in ophthalmology, dermatology, and pulmonology. Our turnkey model activates sites in weeks, maintains strong protocol discipline, and consistently achieves or exceeds enrollment expectations in diverse communities across the United States.
Trusted By Leading Pharma Sponsors and CROs
About Us
Macro manages high-performing research sites in community-based practices. We connect sponsors to experienced clinicians who deliver reliable enrollment, high-quality data, and access to patient populations often missed by traditional academic centers. With centralized oversight, embedded coordinators, and standardized workflows, Macro offers a predictable and scalable model for Phase 2 and beyond therapeutic and device studies.
Why Macro
Sponsors, clinicians, and patients choose Macro because we offer:
Fast and predictable startup
Reliable enrollment across diverse communities
High quality data supported by centralized oversight
End-to-end operational delivery that removes site burden
Research experienced clinicians who understand real world practice
A scalable model for multisite execution through one partner
Our Model
Macro uses a centralized hub and spoke research model that brings consistency, speed, and quality to every study.
Hub: Centralized Operations
Handles all trial setup and infrastructure:
- Contracting, budgeting, and finance
- Regulatory coordination and IRB submissions
- Equipment procurement and protocol setup
- Standardized workflows and SOPs
- Quality oversight and training
- Vendor and IP management
- Real time monitoring of site performance
Spoke Sites: Community Based Investigators
Where enrollment and patient care happen:
- Experienced clinicians with relevant patient populations
- Embedded Macro coordinators
- Multilingual patient support
- Local access for treatment naive and hard to reach populations
This model gives sponsors the speed and consistency of a unified site while maintaining the reach of real-world community practices.
Built for Sponsors, Clinicians, and Patients
Built for pharma, biotech, and CROs on the quest to accelerate safe and effective therapies
Built for people with everyday commitments—we integrate trials into your life, on your terms
WHAT WE DO
Macro is at the center of your next clinical trial.
We work with sponsors and CROs to execute clinical trials for high-value therapeutics. We create access for diverse candidates and partner with leading clinicians looking to stay on the forefront of care.
Sponsors & CROs
A national network of proven investigators, activated quickly and managed end to end
Macro streamlines site selection, startup, and ongoing oversight to provide predictable performance, reliable timelines, and data you can trust.
Clinicians
A turnkey clinical research operation that enhances your practice without disrupting your workflow.
Investigators gain access to high value trials while Macro manages study startup, budgeting, contracting, and staffing.
Patients
Access to leading therapies close to home.
Macro sites expand availability of advanced treatments, offer free evaluations, and maintain strong retention through coordinated support.
What People are Saying
"During Covid, Macro was able to quickly pivot and put patients above everything. Macro's staff went to such great lengths to set up satellite sites at the drop of a hat and see patients in other states."
Melissa Summers
Clinical Trials Team Manager
Synteract®
"I recommend any physician looking to engage in clinical trials to consider partnering with Macro.”
Roxann Becco, RN
Director Clinical Operations
Horizon Therapeutics
"Macro could not have been more accommodating with times, tests, and creating a truly warm and receptive environment for patient participants."
Jeanne
Patient
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 trials, including complex biologics and interventional protocols. This drives predictable performance across Phase 2 and Phase 3 programs.
Fast activation and disciplined operational delivery
Macro’s centralized contracting, regulatory, and logistics model shortens startup timelines and ensures every site begins with the right equipment, staff, and workflow in place.
Reliable enrollment and strong retention
Our embedded coordinators and community-based clinicians reach patients who are often missed by traditional sites. Macro sites consistently achieve or exceed enrollment targets and can reach treatment-naïve patient populations through our nationally footprint.
Access to diverse real world patient populations
Macro’s partners reach communities with broad demographic representation. We support inclusion of underrepresented patients in ophthalmology, pulmonology, and dermatology studies.
End to end site support that removes burden from investigators
Macro manages budgeting, contracting, equipment procurement, IRB coordination, coordinator staffing, and visit logistics. Clinicians focus on oversight and care, while Macro ensures quality and compliance.
Study ready infrastructure that supports consistent high-quality data
Central oversight, experienced coordinators, and standardized workflows enable clean data collection and near perfect protocol adherence across studies.