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Clinical Research Coordinator

No-Resistance Consulting Group
Posted 2 days ago, valid for 18 days
Location

Tuscaloosa, AL, US

Salary

$22.5 - $25 per hour

Contract type

Full Time

Health Insurance
Paid Time Off

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Sonic Summary

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  • No Resistance is seeking motivated individuals to join their team in Tuscaloosa, AL, with an expected start date in October.
  • The position offers a competitive salary ranging from $22.50 to $25.00 per hour for full-time hours of 40 per week, Monday to Friday.
  • No prior clinical trial experience is required, as No Resistance will provide training for the right candidates.
  • Key responsibilities include maintaining regulatory binders, recruiting study subjects, collecting samples, and ensuring protocol compliance.
  • This role is particularly suited for senior pre-medical students or recent graduates looking to gain experience in clinical research before medical school.

Job Location:

Tuscaloosa, AL 

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 may vary based on clinic hours and studies. 

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




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