Clinical Research Coordinator

No Resistance Consulting Group, LLC.

Dallas (TX)

On-site

USD 52,000 - 56,000

Full time

14 days+
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Benefits offered by this job

401(k)
Dental Insurance
Health Insurance
Paid time off
Vision Insurance

Job summary

No Resistance Consulting Group, LLC is seeking motivated individuals to join our team in Dallas, Texas as clinical research staff. In this role, you'll help implement and execute clinical projects to ensure quality, safety, regulatory compliance, and budget objectives.

No prior clinical trial experience is required; training is provided. The position is full-time, Monday–Friday, 8:30 am to 5:00 pm, in person, with a 40-hour workweek and a pay rate of $25.00 per hour.

Qualifications

  • No clinical trial experience is required; training is provided.
  • 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.

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.

Job description

Job Location:

Dallas, Texas

Expected Start Date:

October 1st

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: $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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