Clinical Research Coordinator No-Resistance Consulting Group - 4.4 Baton Rouge, LA Job Details Full-time $22.50 - $25.00 an hour 1 hour ago Benefits Health insurance Dental insurance 401(k) Paid time off Vision insurance Qualifications Direct patient care Maintaining an organized workspace Informed consent Regulatory compliance Healthcare practice inventory management Research project coordination Collecting samples for laboratory testing Clinical data entry Informed consent procedures implementation Research compliance clinical trial records management Implementing research protocols Patient recruitment Care facility supply management Data collection Research participation Ordering supplies Entry level Quality data entry Under 1 year Research compliance quality assurance records management

PCR Full Job Description 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 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:

Maintaining regulatory binders, inventory of study-specific and clinical supplies. Recruiting, and enrolling study subjects. Obtaining informed consent. Collecting nasal swab samples. Testing samples on investigational laboratory PCR analyzers. Data collection and entry. Query resolution. Assuring protocol compliance and efficient workflow including organizing clinical work areas, tracking and ordering study supplies and shipping materials, checking and replacing expired items, etc.

Key Success Factors:

Ability to work independently. Desire to work in a clinical environment with direct patient contact. Genuine interest in research. Timely in all communications. Superior attention to detail. 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:

$22.50- $25.00 per hour Expected hours: 40 per week

Benefits:

401(k) Dental Insurance Health Insurance Paid time off

Vision Insurance Schedule:

Monday to

Friday Work Location:

In person