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Clinical Trial Nurse - Per Diem Portland, OR

IQVIA

Clinical Trial Nurse - Per Diem Portland, OR

part-timePosted: Aug 14, 2026Updated: Sep 1, 2026United States, Oregon, Portland

Job Description

Clinical Trial Nurse – Per Diem – Portland, ORWork Set-Up: Local Travel – In-Home Patient VisitsJob Type: Per DiemAbout the RoleIQVIA 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.Key ResponsibilitiesConduct in‑home visits with clinical trial participantsPerform study‑related procedures in accordance with protocol requirementsCollect and process biological samples and clinical data, including:Blood drawsVital signs and urine testingSubcutaneous medication administration (when required)Label, package, and ship specimens per protocolAccurately document visit data, adverse events (AEs), and serious adverse events (SAEs)Complete mental health (MH) reviews when applicableCommunicate effectively with study teams and patients to ensure compliance and safetySchedule & Travel RequirementsFlexible per‑diem scheduleVisits typically occur in the morning or early afternoonRegional travel required (up to 90 miles)Reliable transportation is requiredRequired QualificationsActive RN license in the state where work is performedBLS certificationRecent and demonstrated blood draw experienceHematology experienceComfortable using basic computer and documentation systemsAbility to work independently in a home‑based care settingReliable transportation, mobile phone, and internet accessPreferred QualificationsPediatric nursing experiencePrevious exposure to clinical trials or research nursingWhy Join IQVIAFlexible scheduling that fits your lifestyleOpportunity to work locally while expanding your clinical skill setExposure to clinical research and trial operationsCompetitive per‑diem compensationAdditional InformationThis role is per‑diem and not eligible for full‑time benefitsSponsorship is not available for this position#LI-CES #LI-DNP #LI-HCPIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.comIQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoeIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.The potential base pay range for this role is $50.00-$60.00 per hour. The 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 benefits.

Locations

  • United States, Oregon, Portland

Required Qualifications

  • Label, package, and ship specimens per protocol (experience)
  • Accurately document visit data, adverse events (AEs), and serious adverse events (SAEs) (experience)
  • Complete mental health (MH) reviews when applicable (experience)
  • Communicate effectively with study teams and patients to ensure compliance and safety (experience)
  • Flexible per‑diem schedule (experience)
  • Visits typically occur in the morning or early afternoon (experience)
  • Regional travel required (up to 90 miles) (experience)
  • Reliable transportation is required (experience)
  • Flexible per‑diem schedule (experience)
  • Visits typically occur in the morning or early afternoon (experience)
  • Active RN license in the state where work is performed (experience)
  • BLS certification (certification)
  • Recent and demonstrated blood draw experience (experience)
  • Hematology experience (experience)
  • Comfortable using basic computer and documentation systems (experience)
  • Ability to work independently in a home‑based care setting (experience)
  • Reliable transportation, mobile phone, and internet access (experience)
  • Active RN license in the state where work is performed (experience)

Preferred Qualifications

  • Pediatric nursing experience (experience)
  • Previous exposure to clinical trials or research nursing (experience)
  • Pediatric nursing experience (experience)
  • Previous exposure to clinical trials or research nursing (experience)

Responsibilities

  • 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 drawsVital signs and urine testingSubcutaneous 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
  • 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:
  • Vital signs and urine testing

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