Clinical Research Nurse - Home Visits (PRN); New Orleans, Louisiana

Are you a skilled, compassionate nurse looking for flexible work in clinical research? As a Clinical Research Nurse - Home Visits (PRN), you'll provide high-quality nursing care directly in patients' homes while supporting important research studies. This role is ideal for nurses who value flexibility, independence, enjoy local travel, and want to supplement their income with meaningful work. Key Points to Know: This is a part-time/per diem position Work is project-based and PRN/per diem - there is no guarantee of hours or assignments Project timelines and frequency vary based on study needs and geographic location You'll use your own vehicle to visit patients in their homes, typically within 1-2 hours of your location Study-specific orientation and materials are provided to support protocol requirement Compensation includes time spent on visits, travel and required documentation (per project terms) Position: Clinical Research Nurse - Home Visits (PRN) Job Type: Employee (W2), PRN, Part-time/Per Diem Hourly Rate: $55/hr onsite and $50/hr travel time Work Location: New Orleans, Louisiana; Drive up to 1-2 hours to patient homes in your area (travel time compensated!) Job Description: As a Clinical Research Nurse - Home Visits (PRN), you will support clinical trial patients in their homes by performing study-related procedures and ensuring protocol compliance. This role requires a high level of independence, attention to detail, and commitment to patient safety and data integrity. Principal Duties and Responsibilities: Provide high-quality nursing care to clinical trial participants in their homes Perform study-related procedures, including but not limited to: Vital signs Specimen collection, processing, and shipment Electrocardiograms (ECGs) Process specimens and ship specimens per protocol. Administer investigational medications/products per study protocol Conduct patient assessments and monitor for adverse events; report findings to the study team/Principal Investigator Accurately document all visit activities in accordance with study requirements Educate patients on study procedures, medications, and compliance Maintain adherence to ICH-GCP guidelines and study protocols Communicate effectively with patients, caregivers, and study teams Maintain strict adherence to HIPAA and all applicable patient privacy regulations, ensuring secure handling and confidentiality of protected health information (PHI) Act as an advocate for patients/participants and their families Work autonomously, recognize limitations, and escalat… Follow ethical research requirements, including protections for vulnerable populations Qualifications: Active, unrestricted nursing licensure Graduate from an accredited BSN or Associate Degree in Nursing or Nursing Diploma program Minimum 2 years’ post qualification acute care experience Clinical Research experience preferred BLS certification required ICH-GCP Certificate (or willingness to obtain) Basic IT proficiency (mobile devices, documentation systems, Microsoft tools) Ability to work independently in home-based settings Valid driver's licenses and reliable transportation Trained in Handling and Transport of Hazardous Substances (training can be provided) Flexible schedule is essential Highlights: Compensation is project-based and may vary by state Flexible scheduling based on project availability Paid travel time and mileage reimbursement (per contract terms) Opportunities to expand clinical research experience The ability to contribute to innovative, patient-centered clinical trials Join our network of independent clinical research nurses and help bring clinical research directly to patients, improving access and advancing medical innovation. What Sets Us Apart: Compensation is project-based and may vary by state Flexible scheduling based on project availability Paid travel time and mileage reimbursement (per contract terms) Opportunities to expand clinical research experienceThe ability to contribute to innovative, patient-centered clinical trials How We Work at WEP Clinical: At WEP Clinical, we look for individuals who are conscientious, exercise sound judgment, and engage with others thoughtfully and professionally. We believe excellence is achieved through integrity, accountability, and respect for diverse perspectives - and we are committed to helping our people grow and succeed in an inclusive, supportive environment. Data Privacy Notice: WEP Clinical is committed to protecting your personal information throughout the recruitment process. By applying, you acknowledge that your personal data will be processed in accordance with our Privacy Policy and Job Applicant Privacy Notice. Privacy Policy: Job Applicant Privacy Notice: For Your Safety, Please Note: We will never communicate with you via Microsoft Teams or text message We will never ask for your bank account information at any stage of recruitment WEP Clinical is a smoke-free, drug-free, and alcohol-free work environment. WEP Clinical is an equal-opportunity employer. WEP Clinical does not unlawfully discriminate against employees or applicants for employment based on an individual’s race, colour, religion, creed, sex, sexual orientation, gender identity or expression, national origin, genetic information, age, disability, marital status, veteran status or any other status protected by applicable law. This policy applies to all terms, conditions, and privileges of employment, including recruitment, hiring, placement, compensation, promotion, discipline, and termination. WEP Clinical will make reasonable accommodation for qualified individuals with known disabilities, in accordance with applicable law. #J-18808-Ljbffr