Clinical Trial Nurse - Per Diem Nashville, TN
About The Position
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. IQVIA 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. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.
Requirements
- 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
Nice To Haves
- Pediatric nursing experience
- Previous exposure to clinical trials or research nursing
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 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
Benefits
- Flexible scheduling that fits your lifestyle
- Opportunity to work locally while expanding your clinical skill set
- Exposure to clinical research and trial operations
- Competitive per-diem compensation
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Part-time
Career Level
Mid Level
Education Level
Associate degree
Number of Employees
5,001-10,000 employees
