Clinical Research Nurse - Home Visits (PRN); Nashville and Eastern Tennessee
Nashville, TennesseePart Time Per DiemPosted Oct 19, 2026
Requirements at a glance
Clinical Research Nurse - Home Visits (PRN); Nashville and Eastern Tennessee at WEP Clinical is a role based in Nashville, Tennessee. The posting asks for 2+ years of experience. It does not mention visa sponsorship. Key skills include Google Cloud and Basic Life Support (BLS). Applications are submitted through Lever.
- Experience
- 2+ years
- Visa sponsorship
- Not mentioned in the posting
- Application platform
- Lever
Skills in this posting
- Google Cloud
- Basic Life Support (BLS)
Extracted automatically from the job description. Confirm details in the full posting below.
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: Nashville and Eastern Tennessee; 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.
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:
WEP Clinical partners with biopharmaceutical Sponsors to help them bring treatments closer to the patients who need them most. Through end-to-end clinical trial delivery, home health services, expanded access programs, and market access consultancy, we provide flexible, fit-for-purpose solutions that support drug development, improve access, and help therapies reach the right patients at the right time. With more than 15 years of global experience, we have supported programs across 150+ countries, combining operational scale with the agility and personalized service of a specialized provider. Our work helps bridge critical gaps in care, ensuring safe, ethical, and efficient access to promising new treatments.
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: https://www.wepclinical.com/privacy-policy/
Job Applicant Privacy Notice: https://www.wepclinical.com/Job-Applicant-Privacy-Notice/
How to Apply:
To be considered for this role, please submit your resume through the WEP Clinical Careers Portal or by using LinkedIn’s Easy Apply option. Please ensure your resume is in English.
Important Note:
To streamline our hiring process, we use an Upwage AI screener. If you receive a link from Upwage, it is a legitimate part of our application process and helps ensure every candidate is reviewed consistently. If you are selected to move forward after the screener, a member of our team will contact you directly from an @wepclinical.com email address to guide you through the next steps of the interview process. Please ensure you apply only through our official careers page (https://www.wepclinical.com/careers/) or our verified LinkedIn page.
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.
Principal Duties and Responsibilities:
- 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 escalate concerns appropriately
- Follow ethical research requirements, including protections for vulnerable populations