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No Resistance Consulting Group

No Resistance has the required experience, expertise, people, and resources to enable urgent care centers (even those with no previous clinical trial experience) to participate in vital clinical trials and add an ancillary income source. No Resistance starts by recruiting and vetting experienced urgent care operators who not only have access to the desired patient base but also have a genuine interest in participating in research and contributing to the common good. We then contract with sponsors whose trial protocols seek to recruit subjects that closely match our clinic populations and clinical presentations. We then contract with the trial sites and embed No Resistance employed experienced investigators and/or study coordinators within the urgent care practices. This business model virtually eliminates the clinic's administrative and time burden and enables our sites to maximize subject enrollment – without adversely affecting the clinic’s normal workflow. It is a win/win/win for No Resistance, the sponsor, and the trial site. We pay the urgent care site a portion of the subject-specific fees for each subject that is enrolled in the trial at their clinic. A pretty simple idea, highly effective. Urgent care patients universally express that their participation in these trials is a very positive component of their patient experience and consider urgent care clinics participating in research to be “cutting edge”.

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Research Services 31 Employees Found Birmingham, United States Founded 2016 145321 Similar Companies
31 Employees Found
86% Email Coverage
$992.0K Est Revenue
1 Office HQ
145321 Similar Companies
Jul '26 Last Verified

No Resistance Consulting Group – Company Information

Research Services
Founded 2016
4425 Sicard Hollow Rd, Birmingham, Alabama, 35242, US
Research Pharmaceutical Clinical Trials Regulatory Enrollment Diagnostics Participation Clinical Research Medical Device Urgent Care GCP CRC UC Medical Research Vaccine Good Clinical Practice Sponsor Ancillary Income Clean Data Clinical Study Principal Investigator High Enrollment Point of Care Clinical Trials Trial Site Management Clinical Research Coordinator Study Coordinator Investigational Product Clinical Research Trial

Frequently asked questions about No Resistance Consulting Group

What is No Resistance Consulting Group email format?

The widely used No Resistance Consulting Group email format is {first_initial}{last} (e.g. jsmith@no-resistance.com) with 75.00% adoption across the company.

What is No Resistance Consulting Group customer service number?

To contact No Resistance Consulting Group customer service number in your country click here to find.

Who are the decision makers in No Resistance Consulting Group?

The decision makers in No Resistance Consulting Group are Danielle Otmaskin, Glenn Harnett, Ryan Mccrory, etc. Click to Find No Resistance Consulting Group decision makers emails.

What types of clinical trials does No Resistance Consulting Group support?

No Resistance Consulting Group specializes in a wide range of clinical trials, including those related to pharmaceuticals, medical devices, vaccines, and diagnostics. We work with urgent care centers to help them participate in vital clinical trials, even if they have no previous experience. Our services encompass all phases of clinical research, ensuring that our clients can effectively engage in studies that align with their capabilities and expertise.

How does No Resistance assist urgent care centers in participating in clinical trials?

No Resistance provides comprehensive support to urgent care centers by offering expertise in trial site management, regulatory compliance, and patient enrollment strategies. We guide centers through the entire process, from initial feasibility assessments to the implementation of Good Clinical Practice (GCP) standards. Our team also trains clinical research coordinators and principal investigators to ensure that all staff are well-prepared to conduct clinical trials successfully.

What are the benefits of participating in clinical trials for urgent care centers?

Participating in clinical trials can provide urgent care centers with several benefits, including ancillary income through trial sponsorships, access to cutting-edge medical research, and the opportunity to contribute to advancements in healthcare. Additionally, involvement in clinical trials can enhance the center's reputation, attract new patients, and provide staff with valuable training and experience in clinical research methodologies.

What is the process for enrolling patients in clinical trials through No Resistance?

No Resistance employs a strategic approach to patient enrollment, which includes identifying eligible patient populations, utilizing targeted outreach methods, and leveraging our extensive network of healthcare professionals. We also provide support in developing patient recruitment materials and conducting community engagement initiatives to raise awareness about the trials. Our goal is to ensure high enrollment rates while maintaining the integrity and quality of the data collected.

What regulatory support does No Resistance offer to clinical trial sites?

No Resistance offers comprehensive regulatory support to ensure compliance with all applicable laws and guidelines. Our team assists with the preparation and submission of regulatory documents, including Institutional Review Board (IRB) applications and Investigational New Drug (IND) submissions. We also provide ongoing support throughout the trial to address any regulatory queries and ensure that the trial adheres to Good Clinical Practice (GCP) standards.

Can No Resistance help with the management of clinical research coordinators and study staff?

Yes, No Resistance provides management and training for clinical research coordinators and study staff. We offer tailored training programs that cover essential topics such as trial protocols, data management, patient interaction, and compliance with regulatory requirements. Our experienced team also assists in the recruitment and onboarding of qualified personnel to ensure that the clinical trial is staffed with skilled professionals who can effectively manage the study.