Dallas, Texas, United States · On-site
$22/hr–$25/hr
Job Location: Dallas, Texas Expected Start Date: October 1st Company Description: Headquartered in Birmingham, No Resistance is a clinical trial site management organization that performs clinical trials in urgent care c…
Skills: Clinical research, Regulatory compliance, Data collection, Data entry, Patient recruitment
Baton Rouge, Louisiana, United States · On-site
$22/hr–$25/hr
Job Location: Baton Rouge, LA Expected Start Date: September 7th 2026 Company Description: Headquartered in Birmingham, No Resistance is a clinical trial site management organization that performs clinical trials in urge…
Skills: Clinical research, Regulatory compliance, Patient recruitment, Informed consent, Sample collection
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The Clinical Research Coordinator is responsible for managing regulatory documentation, recruiting study subjects, and obtaining informed consent. They will also perform nasal swab sample collection, conduct PCR testing, and ensure strict adherence to clinical research protocols.
No prior clinical trial experience is required as the company provides training for the right candidate. Candidates should possess strong attention to detail, the ability to work independently, and a genuine interest in clinical research.
Job Location:
Dallas, Texas
Expected Start Date:
October 1st
Company Description:
Headquartered in Birmingham, No Resistance is a clinical trial site management organization that performs clinical trials in urgent care centers throughout the north and southeast. We focus on sample collection and testing trials for lab device manufacturers with the purpose of collecting data to support the device's 510(k) or emergency use approval by the FDA. Notably, the trials we have participated in have directly led to the FDA EUA approval of three separate COVID-19 PCR testing platforms.
No clinical trial experience is required. No Resistance will train the right candidate(s). Hours are Monday-Friday 8:30 am to 5:00 pm with no weekend requirements.
Job Description:
No Resistance is seeking motivated individuals to join our team! In this role, you'll play a pivotal part in the implementation and execution of clinical research projects, ensuring the successful attainment of quality, safety, regulatory, and financial objectives.
Job Duties:
Key Success Factors:
While not a requirement, senior pre-medical students who hope to gain experience in clinical research or recent graduates who have a "gap" year before they start medical school are encouraged to apply. This position offers an exceptional opportunity to earn a competitive income while gaining invaluable experience highly regarded by medical school admission committees.
Job Type: Full-time
Pay: $25.00 per hour
Expected hours: 40 per week
Benefits:
Schedule:
Work Location: In person
Point of Care Clinical Trial Site Management Services
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”.
Offices: 4425 Sicard Hollow Rd, Birmingham, Alabama 35242, US
Point of Care Clinical Trial Site Management Services
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”.
Offices: 4425 Sicard Hollow Rd, Birmingham, Alabama 35242, US
