Clinical Research Coordinator at No Resistance… · Selden

Summary: No Resistance Consulting Group is a clinical trial site management organization that conducts clinical trials in urgent care centers throughout the north and southeast. The Clinical Research Coordinator will support the implementation and execution of clinical research projects by recruiting and enrolling subjects, collecting and testing samples, managing study data, and ensuring protocol compliance and regulatory objectives.

Responsibilities:
- 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

Required Qualifications:
- No clinical trial experience is required
- 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

Preferred Qualifications:
- Pediatric experience is a plus
- 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

Required Skills: Pediatric Experience

Benefits: 401(k), Dental Insurance, Health Insurance, Paid time off, Vision Insurance