About The Position

The Clinical Research Nurse – Home Visits (PRN) provides nursing care to clinical trial participants in their homes and supports research studies by performing study-related procedures and ensuring compliance with study protocols. The role involves independent work, local travel to patients’ homes—typically within 1–2 hours—and a strong focus on patient safety, accurate documentation, and data integrity. Assignments are project-based, and hours are not guaranteed; project timelines and visit frequency depend on study needs and location. Study-specific orientation and materials are provided. Compensation is $55 per hour for onsite time and $50 per hour for travel time, with mileage reimbursement and other terms subject to project or contract terms. The position is part-time, PRN/per diem, and employee (W2). The nurse uses their own vehicle and may perform procedures such as vital signs, specimen collection and processing, specimen shipment, ECGs, and administration of investigational medications or products. The nurse conducts assessments, monitors and reports adverse events, educates participants, communicates with patients, caregivers, and study teams, and follows applicable research, privacy, and safety requirements. 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 supporting safe, ethical, and efficient access to treatments, and states a commitment to integrity, accountability, respect, and an inclusive, supportive environment. It is an equal-opportunity employer and may use AI tools to assist with parts of recruitment; final hiring decisions are made by humans.

Requirements

  • Active, unrestricted nursing licensure.
  • Graduation from an accredited BSN, Associate Degree in Nursing, or Nursing Diploma program.
  • At least 2 years of post-qualification acute care experience.
  • BLS certification.
  • Ability to work independently in home-based settings.
  • Valid driver’s license and reliable transportation.
  • Basic IT proficiency, including mobile devices, documentation systems, and Microsoft tools.
  • Flexible schedule.
  • Training in handling and transport of hazardous substances, or willingness to complete training provided.
  • ICH-GCP certificate or willingness to obtain one.

Nice To Haves

  • Clinical research experience.

Responsibilities

  • Provide nursing care to clinical trial participants in their homes.
  • Perform study-related procedures, including vital signs, specimen collection and processing, specimen shipment, and 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 and securely handle protected health information in accordance with HIPAA and applicable regulations.
  • 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 and comply with applicable project terms for travel time and mileage reimbursement.

Benefits

  • Paid travel time, subject to project or contract terms.
  • Mileage reimbursement, subject to project or contract terms.
  • Study-specific orientation and materials are provided.
  • Opportunities to expand clinical research experience.
  • Flexible scheduling based on project availability.
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