No Experience Necessary
You Can Become a Clinical Trial Host Site!

We have the experience. You have the patients. Working together, we can both enjoy the professional and economic benefits of conducting clinical trials at your location(s).

WHY SHOULD YOUR CLINIC
BECOME A CLINICAL TRIAL SITE?

We understand that your team needs to be laser-focused on what they do best - safely caring for their patients, minimizing throughput times, and providing a superior patient experience. Partnering with No Resistance allows them to maintain that focus and for you to achieve the financial and professional benefits of participating in vital research.

A Turnkey Process

No Resistance embeds an experienced clinical trial research associate at your clinic who manages all aspects of the trial - from patient screening and consent to sample collection, documentation, & shipping.

Ancillary Income

Clinical Trial Host Sites benefit from a lucrative stream of income with ZERO cash outlay and very little time or effort. We do the work for you!

Minimal Workflow Disruption

We focus on making sure that our trials are minimally disruptive to your site's operational workflow, including ZERO effect on your patient throughput times.

Stand out as a Pioneer in Research

Clinical research helps you stand out from your competitors as a clinic that provides innovative and advanced patient care.

QUESTIONS? LOOK HERE
FREQUENTLY ASKED QUESTIONS

What kind of trials does No Resistance participate in?
We focus on lab device trials for Sponsors who are conducting trials with the hope of getting their devices FDA approved as a CLIA-waived test. Some of the trials are sample collection only (typically nasal or NP swabs) while other include sample collection and subsequent testing of the sample on the sponsor’s device in your clinic.
Do any of our clinic staff or providers need to have previous clinical trial experience to participate?
No, nobody, including your providers need clinical trial experience.
Do we need to provide any of our own staff to participate in clinical trials?
Some of our lab device trials will require that the clinic provide staff members to act as device operators to test collected samples at your clinic. This is a simple and rapid process, that only takes a minute or two to complete.
Are there any requirements or courses required before we begin a trial?
Providers who participate in a clinical trial as a Principal Investigator or Sub-Investigator must complete brief online training courses on Good Clinical Practices and Human Subject Protection. These courses typically only take a few hours to complete.
Interested in working with No Resistance Consulting Group?
Contact us today