Clinical Trial Nurse

IQVIA

McAllen, TXFull-timePosted Apr 29, 2026

Behavioral Health Market Context

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Benefits

Flexible scheduling that fits your lifestyleOpportunity to work locally while expanding your clinical skill setExposure to clinical research and trial operationsCompetitive per‑diem compensationThis role is per‑diem and not eligible for full‑time benefitsSponsorship is not available for this positionThe potential base pay range for this role is $50.00-$60.00 per hourThe actual base pay offered may vary based on a number of factors including job‑related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part‑time)Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits6 more items(s)

Qualifications

  • Flexible per‑diem schedule
  • Regional travel required (up to 90 miles)
  • Reliable transportation is required
  • Active RN license in the state where work is performed
  • BLS certification
  • Recent and demonstrated blood draw experience
  • Hematology experience
  • Comfortable using basic computer and documentation systems
  • Ability to work independently in a home‑based care setting
  • Reliable transportation, mobile phone, and internet access
  • 7 more items(s)

Responsibilities

  • IQVIA is seeking experienced Registered Nurses to support clinical trial activities through in‑home patient visits in the Eugene, OR area
  • This per‑diem role is ideal for nurses seeking flexible, supplemental work while gaining hands‑on experience in clinical research
  • As a Clinical Trial Nurse, you will play a critical role in ensuring patient safety and high‑quality data collection that supports the development of innovative treatments
  • This position involves local and regional travel and requires comfort working independently in patients’ homes while adhering to study protocols and regulatory standards
  • Conduct in‑home visits with clinical trial participants
  • Perform study‑related procedures in accordance with protocol requirements
  • Collect and process biological samples and clinical data, including:
  • Blood draws
  • Vital signs and urine testing
  • Subcutaneous medication administration (when required)
  • Label, package, and ship specimens per protocol
  • Accurately document visit data, adverse events (AEs), and serious adverse events (SAEs)
  • Complete mental health (MH) reviews when applicable
  • Communicate effectively with study teams and patients to ensure compliance and safety
  • Schedule & Travel Requirements
  • Visits typically occur in the morning or early afternoon
  • 13 more items(s)


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