Clinical Research Nurse - Home Visits (PRN); New Orleans, Louisiana
About The Position
The Clinical Research Nurse provides nursing care to clinical trial participants in their homes and supports research studies by performing study-related procedures and ensuring protocol compliance. The role requires independence, attention to detail, and a commitment to patient safety and data integrity. Patient visits are typically within one to two hours of the nurse’s location, using the nurse’s own vehicle. Work is project-based and PRN/per diem, with no guaranteed hours or assignments; timelines and frequency vary according to study needs and geography. Study-specific orientation and materials are provided. Compensation covers onsite visit time and travel time, with mileage reimbursement according to project terms. The position is part-time/per diem and employee (W2). The listed rates are $55 per hour onsite and $50 per hour for travel time. The role is based in the New Orleans, Louisiana area.
Requirements
- Active, unrestricted nursing licensure.
- Graduate of an accredited BSN, Associate Degree in Nursing, or Nursing Diploma program.
- At least two years of post-qualification acute care experience.
- BLS certification.
- ICH-GCP certificate or willingness to obtain one.
- Basic IT proficiency, including mobile devices, documentation systems, and Microsoft tools.
- Ability to work independently in home-based settings.
- Valid driver’s license and reliable transportation.
- Training in handling and transporting hazardous substances, or willingness to complete training provided for the role.
- Flexible schedule.
Nice To Haves
- Clinical research experience.
Responsibilities
- Provide high-quality nursing care to clinical trial participants in their homes.
- Perform study-related procedures, including vital signs, specimen collection, processing and shipment, and electrocardiograms (ECGs).
- Administer investigational medications or products in accordance with study protocols.
- Conduct patient assessments, monitor for adverse events, and report findings to the study team or Principal Investigator.
- Accurately document visit activities in accordance with study requirements.
- Educate patients about study procedures, medications, and compliance.
- Adhere to ICH-GCP guidelines and study protocols.
- Communicate effectively with patients, caregivers, and study teams.
- Protect patient privacy by following HIPAA and applicable privacy regulations and securely handling protected health information.
- Advocate for patients, participants, and their families.
- Work autonomously, recognize limitations, and escalate concerns appropriately.
- Follow ethical research requirements, including protections for vulnerable populations.
Benefits
- Paid travel time and mileage reimbursement, according to project terms.
- Flexible scheduling based on project availability.
- Opportunities to expand clinical research experience.
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What This Job Offers
Job Type
Part-time
Career Level
Mid Level
Education Level
Associate degree
