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Sponsors & CROs

Precision Execution for Your Next Clinical Trial.

A clinical trial site for sponsors and CROs delivering reliable data integrity, predictable recruitment, and rapid startup metrics across diverse therapeutic areas.

Rapid Startup
24–48Hr
Regulatory Turnaround
Patient-Centricity
90%+
Retention Standard TARGET
Quality & Compliance
100%
GCP & FDA SOP Adherence
Operational Support
1:1
Embedded CRC Coverage
Capabilities

Equipment & on-site capabilities.

Our site is equipped to process samples, monitor participants and manage data to protocol, with dedicated space for sponsor and CRA visits.

01

Processing & Storage Infrastructure

  • Centrifuges (Ambient & Refrigerated)
  • -80°C and -20°C Locked, Monitored Freezers with 24/7 Temperature Logging & Alarm Systems
  • Locked, Controlled Room-Temperature Drug Storage Cabinets
02

Diagnostic & Monitoring Equipment

  • 12-Lead ECG Machines with Digital Transmission
  • On-Site Laboratory Draw & Sample Processing Stations
  • Calibrated Medical Scales, Stadiometers, and Vital Signs Monitors
  • Emergency Safety Equipment: Crash Carts, Automated External Defibrillators (AEDs), and Supplemental Oxygen Supplies
03

Data Management & Systems

  • HIPAA-Compliant Electronic Source / eCRF Integration
  • Secure High-Speed Internet Infrastructure for Remote Monitoring / EDC Systems
  • Dedicated Private Workstations for CRA (Monitor) On-Site Visits
Therapeutic Areas

Therapeutic areas of expertise.

01

Primary & Internal Medicine

General Internal Medicine & Primary Care

02

Endocrinology

Metabolic Disorders, Type 1/2 Diabetes, Obesity, NASH/NAFLD

03

Cardiovascular

Hypertension, Cardiovascular Risk Reduction, Heart Health

04

Neurology

Neurological Conditions, Pain Management, Cognitive Impairment

05

Respiratory

Asthma, COPD, Chronic Allergy Management

06

Specialty Care

Women’s Health

Facilities

Sites built for research.

Our clinic combines routine patient care with dedicated research infrastructure, so studies run smoothly alongside everyday practice.

Monitoring

Dedicated CRA Workstations

Private workstations for monitors during on-site visits, with secure high-speed internet for EDC systems.

Storage

Secure Drug & Sample Storage

Locked, temperature-monitored freezers and drug storage with 24/7 logging and alarm systems.

Safety

Emergency-Ready Clinics

Crash carts, AEDs and supplemental oxygen on-site for participant safety.

Staffing

Embedded Coordinators

Full-time, experienced CRCs integrated directly on-site to handle trial workflows.

Clinical research site in Oak Forest, Illinois
6300 W 159th St Suite A, Oak Forest, IL 60452 · 708.289.3032

Study Startup

From protocol to first patient in.

Single-point-of-contact contracting, central IRB reliance, and streamlined budget negotiations minimize cycle time at every step.

1

Protocol Delivery

Share your protocol with one point of contact who manages feasibility and coordination from day one.

2

Contracting & Budget

Single-point-of-contact contracting with swift budget and CTA negotiation.

3

Central IRB Reliance

Accelerated regulatory review through central IRB reliance.

24–48 HR TURNAROUND
4

First Patient In

Dedicated recruitment teams and embedded CRCs move quickly to enrollment and First Patient In (FPI).

Pipeline

Our study pipeline.

We are actively partnering with sponsors and CROs on upcoming studies. Request our current pipeline and site availability for your therapeutic area.

Sponsor Inquiry

Submit a protocol or start a conversation.

Tell us about your study and our team will follow up with feasibility, site capabilities and startup timelines.

  • Phone[Phone number]
  • Email[Email address]
  • Office[Street address, City, State ZIP]

Please do not include patient health information in this form.