Clinical Research Coordinator
$22.5 - $25 per hourNo-Resistance Consulting Group
Job Location: Baton Rouge
Expected Start Date: October 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. Hours will depend on Clinic hours and clinical trial needs.
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:
Work Location: In person
Expected Start Date: October 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. Hours will depend on Clinic hours and clinical trial needs.
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.
- 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.
- 401(k)
- Dental Insurance
- Health Insurance
- Paid time off
- Vision Insurance
- Monday to Friday
Work Location: In person
Vacancy posted 1 day ago
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