Clinical Research Coordinator - Patient-Facing Trials

No Resistance Consulting Group, LLC.

Haverhill (MA)

On-site

USD 30,000 - 34,000

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 clinical research team in Haverhill, MA. You will play a pivotal role in the implementation and execution of clinical research projects, ensuring the successful attainment of quality, safety, regulatory, and financial objectives.

Responsibilities include maintaining regulatory binders, recruiting and enrolling subjects, obtaining informed consent, collecting nasal swab samples, testing samples on PCR analyzers, data

Qualifications

  • No clinical trial experience required.
  • No Resistance will train the right candidate(s).
  • Hours are Monday-Friday 8:30 am to 5:00 pm with no weekend requirements.
  • Desire to work in a clinical environment with direct patient contact.
  • 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 including organizing clinical work areas, tracking and ordering study supplies and shipping materials, checking and replacing expired items, etc.

Job description

No Resistance Consulting Group, LLC is seeking motivated individuals to join our clinical research team in Haverhill, MA. You will play a pivotal role in the implementation and execution of clinical research projects, ensuring the successful attainment of quality, safety, regulatory, and financial objectives.

Responsibilities include maintaining regulatory binders, recruiting and enrolling subjects, obtaining informed consent, collecting nasal swab samples, testing samples on PCR analyzers, data

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