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Clinical Research Coordinator

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

Greenbelt, MD, 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 for a full-time role in clinical trial management at PM Pediatric Urgent Care in Greenbelt, Maryland, starting in October.
  • The position involves implementing and executing clinical research projects, including maintaining regulatory binders, recruiting study subjects, and collecting samples.
  • Candidates are not required to have prior clinical trial experience, as training will be provided, although pediatric experience is a plus.
  • The job offers a competitive salary ranging from $22.50 to $25.00 per hour for a 40-hour work week, with benefits including health insurance and paid time off.
  • This opportunity is ideal for senior pre-medical students or recent graduates looking to gain valuable experience in a clinical environment.

Job Location:

PM Pediatric Urgent Care, Greenbelt Maryland 

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. Pediatric Experience is a plus. Hours may vary based on clinical trial and clinic hours. 

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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