Clinical Research Nurse - Asthma Trial (Contract)

Medix Staffing Solutions, Inc.

Overland Park (KS)

On-site

USD 41,000 - 62,000

Full time

30 hours ago
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Job summary

Medix Staffing Solutions, Inc. seeks an experienced Clinical Research Nurse (RN) to support a full-time, single-protocol asthma study in the Overland Park, KS area. The role combines nursing assessments, patient safety advocacy, trial coordination, and regulatory maintenance.

You will perform spirometry, manage ISF/IRB submissions, data entry in Veeva EDC, and ensure adherence to GCP and FDA guidelines. This is a project-based contract with standard 40-hour weeks, Monday to Friday.

Qualifications

  • Active RN license (Kansas or compact multistate).
  • 2+ years of experience as a Clinical Research Nurse/Coordinator in sponsor-funded trials.
  • Strong nursing clinical assessment skills.
  • Hands-on regulatory experience with ISF/IRB submissions.
  • Experience with lab specimen processing and spirometry testing.
  • Proficient with EHR and CTMS systems.
  • Solid knowledge of FDA regulations, ICH guidelines, and Good Clinical Practice (GCP).

Responsibilities

  • Recruitment and patient outreach to identify eligible participants.
  • Obtain informed consent and prepare patients for visits.
  • Perform nursing assessments and protocol procedures, including spirometry.
  • Handle lab processing tasks and specimen workflow.
  • Maintain regulatory documentation (ISF, IRB submissions, safety updates).
  • Enter data in EDC systems (Veeva EDC) and manage scheduling/reminders.

Skills

Nursing assessment
Regulatory compliance
Lab processing
Spirometry testing
EHR/CTMS software

Job description

Medix Staffing Solutions, Inc. seeks an experienced Clinical Research Nurse (RN) to support a full-time, single-protocol asthma study in the Overland Park, KS area. The role combines nursing assessments, patient safety advocacy, trial coordination, and regulatory maintenance.

You will perform spirometry, manage ISF/IRB submissions, data entry in Veeva EDC, and ensure adherence to GCP and FDA guidelines. This is a project-based contract with standard 40-hour weeks, Monday to Friday.

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