About The Position

The Clinical Research Nurse provides nursing care to clinical trial participants in their homes and supports study procedures, protocol compliance, patient safety, and data integrity. The position is PRN, part-time/per diem, and project-based, with no guarantee of hours or assignments. Study timelines and visit frequency vary by study needs and location. Nurses travel in their own vehicles to patient homes, typically within one to two hours of their location. Study-specific orientation and materials are provided. Compensation covers visit time and travel time according to project terms; the posting also states an hourly rate of $55 for onsite work and $50 for travel time, with mileage reimbursement per contract terms. The role requires independent work in home-based settings, sound judgment, attention to detail, and appropriate escalation of concerns. Nurses must follow study protocols, ICH-GCP guidelines, ethical research requirements, HIPAA, and other applicable privacy regulations. WEP Clinical describes its work as supporting biopharmaceutical sponsors through clinical trial delivery, home health services, expanded access programs, and market access consultancy. The company emphasizes integrity, accountability, respect for diverse perspectives, and an inclusive, supportive environment.

Requirements

  • Active, unrestricted nursing licensure.
  • Graduation from 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; training can be provided.
  • Flexible schedule.

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, processing and shipment, and electrocardiograms (ECGs).
  • 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 according to 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 securely handling and maintaining the confidentiality of 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.

Benefits

  • Paid travel time and mileage reimbursement according to project or contract terms.
  • Flexible scheduling based on project availability.
  • Opportunities to expand clinical research experience.
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service