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 escalate concerns appropriately
- 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
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