Clinical Research Coordinator
About The Position
No Resistance is seeking a Clinical Research Coordinator to help implement and execute clinical research projects at Patient Plus Urgent Care in Brusly. The role supports quality, safety, regulatory, and financial objectives. The company conducts clinical trials in urgent care centers, focusing on sample collection and testing trials for laboratory device manufacturers to support FDA 510(k) or emergency use approval. No clinical trial experience is required; training will be provided. The position is in person, Monday through Friday, 8:30 a.m. to 5:00 p.m., with no weekend requirements. It is full-time at 40 hours per week and pays $25.00 per hour. The expected start date is November 30, 2026.
Requirements
- Ability to work independently.
- Desire to work in a clinical environment with direct patient contact.
- Genuine interest in research.
- Timely communication.
- Superior attention to detail.
Nice To Haves
- Senior pre-medical students seeking clinical research experience are encouraged to apply.
- Recent graduates taking a gap year before medical school are encouraged to apply.
Responsibilities
- Maintain regulatory binders and inventories of study-specific and clinical supplies.
- Recruit and enroll study subjects.
- Obtain informed consent.
- Collect nasal swab samples.
- Test samples on investigational laboratory PCR analyzers.
- Collect and enter data.
- Resolve queries.
- Ensure protocol compliance and efficient workflow, including organizing clinical work areas, tracking and ordering study supplies and shipping materials, and checking and replacing expired items.
Benefits
- 401(k)
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
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What This Job Offers
Job Type
Full-time
Education Level
No Education Listed
