
Clinical Research Nurse – Home Visits
Posted Oct 20

Posted Oct 20
This is a fully remote position, open to applicants in Tennessee.
• Deliver exceptional nursing care to participants in clinical trials within their residences.
• Execute study-related tasks, including taking vital signs, collecting and processing specimens, shipping samples, and conducting ECGs.
• Administer investigational drugs/products in accordance with study protocols.
• Perform patient evaluations and monitor for any adverse reactions; communicate findings to the study team and Principal Investigator.
• Meticulously document all activities conducted during visits in line with study requirements.
• Inform patients about study procedures, medications, and adherence to protocols.
• Ensure compliance with ICH-GCP guidelines and study protocols.
• Engage in effective communication with patients, caregivers, and research teams.
• Uphold HIPAA standards and ensure the secure management of protected health information.
• Serve as an advocate for patients/participants and their families.
• Operate independently, recognizing personal limitations and appropriately escalating concerns.
• Adhere to ethical research standards, including safeguards for vulnerable populations.
• Possession of an active and unrestricted nursing license.
• Graduation from a recognized BSN program, Associate Degree in Nursing, or a Nursing Diploma program.
• A minimum of two years of acute care experience following qualification.
• Current BLS certification is mandatory.
• ICH-GCP Certificate is preferred; willingness to obtain one is acceptable.
• Basic IT skills, including familiarity with mobile devices, documentation systems, and Microsoft applications.
• Capability to work independently in home-based environments.
• A valid driver's license and dependable transportation are required.
• Training in Handling and Transport of Hazardous Substances is preferred, or a willingness to undergo such training.
• Flexibility in scheduling is crucial.
• Experience in Clinical Research is advantageous.
• Compensation encompasses time spent on visits, travel, and necessary documentation as per project terms.
• Paid travel time and mileage reimbursement provided according to contract terms.
• Flexible scheduling based on the availability of the project.
• Orientation and study-specific materials will be supplied.
• Opportunities to enhance clinical research experience.
• Chance to contribute to innovative, patient-centered clinical trials.
Parexel
ICON plc
AbbVie
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