Overnight Research Nurse & Study Coordinator

Tranquil Clinical Research and Consulting Services

Webster (TX)

On-site

USD 52,000 - 78,000

Part time

4 days ago
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Job summary

Tranquil Clinical Research and Consulting Services is seeking a PRN Research Nurse/Coordinator to support overnight, weekend, and holiday study visits. The role operates in an office setting, aligned with the principal investigator, and requires thoughtful patient care and efficient coordination of trial activities.

The ideal candidate will have RN or LPN licensure with clinical trial exposure, familiarity with FDA/GCP, strong organizational skills, and the ability to work independently while

Qualifications

  • RN or LPN with related clinical experience.
  • Minimum 1 year of clinical trials experience.
  • Knowledge of FDA regulations and GCP.
  • Accuracy, attention to detail and ability to set priorities and meet deadlines.
  • MS Office Suite (Word, PowerPoint, Excel)

Responsibilities

  • Coordinate and perform study visits under PI supervision.
  • Review inclusion/exclusion criteria with subjects and obtain informed consent.
  • Ensure regulatory documentation and source data are accurate and complete.
  • Monitor subject safety and report adverse events as required.
  • Maintain study-related logs, schedules, and communications with staff and PI.

Skills

RN/LPN with clinical experience
Clinical trials experience (1 year)
FDA regulations and GCP
Attention to detail and prioritization
MS Office (Word, Excel, PowerPoint)
Excellent bedside manner
Time management and social skills
Detail-oriented and proactive problem‑

Job description

Tranquil Clinical Research and Consulting Services is seeking a PRN Research Nurse/Coordinator to support overnight, weekend, and holiday study visits. The role operates in an office setting, aligned with the principal investigator, and requires thoughtful patient care and efficient coordination of trial activities.

The ideal candidate will have RN or LPN licensure with clinical trial exposure, familiarity with FDA/GCP, strong organizational skills, and the ability to work independently while

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