A Simple introduction of
What we do?
No Resistance contracts with high-volume medical practices such as urgent care clinics to conduct clinical trials at their locations. We are able to tap into this previously untapped source of subject enrollment by embedding one of our experienced clinical research associates in the clinic, thereby eliminating historical barriers to trial participation.
Study Start-up
No Resistance easily navigates new trial sites through the Sponsor site approval process.
Trial/Site Matching
We partner with a variety of Sponsors, allowing us to match appropriate trial opportunities to your unique patient population and workflow.
No experience? No Problem. No Resistance will walk you through the research process, step by step.
All study staff complete GCP, HSP, and IATA training. No Resistance also has an extensive in-house clinical research training program.
MEET OUR
EXECUTIVE TEAM MEMBERS
Glenn Harnett, MD
CEO
Dr. Harnett brings over 20 years of experience as an emergency medicine and urgent care physician. He is an active researcher and has served as a Principal Investigator in numerous clinical trials, including both sponsor-initiated and investigator-initiated studies. His research is centered on advancing original insights in urgent care medicine.
Casey Harnett, MHA
President
Casey brings more than 15 years of executive-level healthcare experience to No Resistance. Recognized as one of the Top 40 Under Forty in 2023, she is a natural leader known for her effortless rapport and prompt communication. Her exceptional ability to foster strong, lasting relationships with our partners has been instrumental to our success.
Bailey Arant, MS
Director of Clinical Operations and Research Strategy
Bailey provides strategic oversight across No-Resistance’s clinical research operations, working closely with research sites, clinical research coordinators, investigators, and study teams to promote efficient, high-quality trial execution. He also supports research strategy, study enrollment, and operational efficiency across the organization while ensuring studies adhere to GCP standards, ethical principles, and the highest standards of participant safety and research integrity.
Maryclare Parker
Director of Trial Management
Maryclare works closely with our Sponsors/CROs and Sites to place studies at our most appropriate Site locations in order to maximize study enrollment. She is also our lead CRC trainer, using her many years of experience at No Resistance to ensure new staff members are ready to hit the ground running.
Seth Maynor, CCRC
Clinical Trial Manager
As an ACRP-certified Clinical Research Coordinator with over five years of experience, Seth plays a key leadership role in ensuring research quality and operational excellence. He directs quality assurance and internal monitoring initiatives designed to strengthen regulatory compliance, improve study performance, and foster accountability. He also manages investigator-sponsored biospecimen collection protocols, providing oversight to support protocol adherence and successful study execution.