About The Position

The Clinical Research Nurse – Home Visits provides nursing care to clinical trial participants in their homes, performs study-related procedures, and supports compliance with study protocols. The role requires independence, attention to detail, and a commitment to patient safety and data integrity. Nurses travel to patients’ homes, typically within one to two hours of their location, using their own vehicle. Project timelines and visit frequency vary with study needs and location, and assignments and hours are not guaranteed. Study-specific orientation and materials are provided. Compensation is project-based and includes $55 per hour for onsite time and $50 per hour for travel time, with mileage reimbursement according to project terms. The position is part-time, PRN/per diem, and project-based. WEP Clinical partners with biopharmaceutical sponsors to deliver clinical trials, home health services, expanded access programs, and market access consultancy. The company describes its work as helping bring treatments closer to patients and supporting safe, ethical access to promising treatments. It values integrity, accountability, respect for diverse perspectives, and an inclusive, supportive environment.

Requirements

  • Active, unrestricted nursing license.
  • Graduate of an accredited BSN, Associate Degree in Nursing, or Nursing Diploma program.
  • At least two years of post-qualification acute care experience.
  • Current 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.
  • Flexible schedule; flexibility is essential.

Nice To Haves

  • Clinical research experience.

Responsibilities

  • Provide high-quality nursing care to clinical trial participants in their homes.
  • Perform study procedures, including vital signs, specimen collection and processing, specimen shipment, and electrocardiograms (ECGs).
  • Process and ship specimens according to study protocols.
  • Administer investigational medications or products according to 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.
  • Travel to patients’ homes using a personal vehicle.

Benefits

  • Flexible scheduling based on project availability.
  • Paid travel time and mileage reimbursement according to project terms.
  • Opportunities to expand clinical research experience.
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