New Jersey Clinical Research Site — Paramus
Advancingmedicine,one volunteerat a time.
We conduct Phase 1–4 clinical trials in Paramus, New Jersey — connecting volunteers with tomorrow's treatments in diabetes, hypertension, Alzheimer's, vaccines, obesity, pulmonary, psychiatry, and cardiology.
The NJCRS commitment
Research built on trust, run with rigor.
Why participate
Clinical trial volunteers gain early access to investigational treatments, receive study-related care at no cost, and help shape the medicines of tomorrow. Every approved therapy exists because someone volunteered first.
Our process
It starts with a simple pre-screening call. Our coordinators walk you through eligibility, informed consent, and every visit — no surprises, no pressure. You can withdraw at any time, for any reason.
Your safety
Every study we run is reviewed by an independent Institutional Review Board and monitored under FDA regulations. Our board-certified investigators oversee your health at every visit.
Studies conducted
Participant visits
Years in Paramus
Therapeutic areas
Currently enrolling
Active studies in Paramus
Each study is registered on ClinicalTrials.gov. Follow the link on any card for the full federal listing.
"Patients first, data always."
Our founding principle
About the site
A dedicated research facility in the heart of Bergen County
New Jersey Clinical Research Site is an independent, investigator-led research facility located at 140 Route 17 North, Paramus, NJ. Our team of board-certified physicians, sub-investigators, and certified clinical research coordinators has partnered with leading pharmaceutical sponsors and CROs for over fifteen years.
Participant voices
In their own words
"The coordinators explained every step before it happened. I never felt like a number — I felt like a partner in the research."
"My mother joined an Alzheimer's study here. The care team treated her with more patience and dignity than I could have hoped for."
"Between visits they checked in constantly. The compensation was fair, but honestly, contributing to a new diabetes treatment meant more."
"I was nervous about my first trial, but the informed consent process answered every question. I've since referred two friends."
Pre-screening
Become a volunteer
Complete this brief interest form and a certified research coordinator will call you to discuss studies you may qualify for. Submitting this form does not obligate you to participate in any study.
01 We review your information confidentially
02 A coordinator calls within 1–2 business days
03 If eligible, we schedule your screening visit
Know someone who might qualify?
Many of our participants come from friend and family referrals. Share this page — referred volunteers who enroll may earn the referrer a thank-you gift.
Common questions
Before you volunteer
Still unsure? Call us at (917) 885-2582 — a coordinator will happily answer anything not covered here.
For sponsors & CROs
Place your next study with a site that delivers
From feasibility to database lock, NJCRS delivers rapid start-up, reliable enrollment, and clean data. Our Paramus location draws from one of the most diverse patient populations in the New York metro area.
< 4 weeks
Median study start-up time
94%
Participant retention rate
120+
Trials completed Phase 1–4
48 hrs
Average query resolution
"Site selection is the single biggest predictor of trial success. We built NJCRS to be the site sponsors come back to."
Site leadership — NJCRS Paramus