Recruitment & Enrollment Capabilities

How CMR moves from protocol to enrolled participants — the database, referral network, outreach channels, and retention support that keep studies on schedule.

1,000+
Phase II–IV Participants Enrolled
10,100+
Recruitment Database Records
250+
Clinical Trial Protocols Executed
2
Chicago-Area Site Locations
35+ Yrs
Combined Investigator Experience

How We Identify Eligible Participants

Our multi-channel recruitment model rapidly surfaces qualifying, diverse participants for Phase II-IV protocols.

Study-Specific Database Prescreening

10,100+ patient records queryable by diagnosis, medication history, lab values, and comorbidities for rapid eligibility identification.

Physician & Practice Referrals

Established referral relationships with cardiology, endocrinology, and internal medicine practices across the greater Chicago area.

Community Outreach

Community events, faith-based partnerships, and local health initiatives connecting diverse, historically underrepresented populations to trials.

Digital Recruitment

Targeted digital advertising, database prescreening, physician referrals, and community-based outreach to surface qualifying participants.

Dedicated Screening & Follow-Up

Trained CRCs conduct informed consent, telephone prescreening, visit scheduling, and protocol-required assessments.

Participant Retention Support

Travel reimbursement, flexible scheduling, reminder calls, and patient-advocacy check-ins throughout the full study lifecycle.

Experience Recruiting Patients with Multiple Chronic Conditions

Many of our participants present with overlapping cardiometabolic conditions — cardiovascular disease, diabetes, obesity, CKD, and hypertension. Our database and physician-referral network allow us to identify these complex patients for protocols requiring multi-morbid populations.

Cardiovascular + Diabetes

CKD + Hypertension

Obesity + Metabolic Syndrome

ASCVD + Dyslipidemia

Prescreen to Retention Workflow

1

Database Query & Prescreen

Run protocol-specific I/E criteria against 10,100+ records.

2

Physician Referral Activation

Activate network physicians for qualifying patients.

3

Outreach & Informed Consent

Contact eligible subjects; complete ICF & screening labs.

4

Enrollment & On-Study Visits

Randomize subjects and execute protocol-required visits.

5

Retention & Follow-Up

Maintain adherence, monitor safety, complete EOS/EOT visits.

Considering CMR for Your Next Study?