Headquartered in Los Angeles, California, Science 37 is a privately held clinical trial and mobile technology company dedicated to accelerating biomedical discovery and reducing th
Per Diem Clinical Research Nurse - Home Visits
Location
United States
Posted
72 days ago
Salary
$50 - $55 / hour
Seniority
Mid Level
No structured requirement data.
Job Description
Per Diem Clinical Research Nurse - Home Visits
Science 37
Science 37’s Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials. Science 37’s extraordinary work environment allows continuous collaboration between clinicians, clinical researchers, patient recruitment specialists, data managers and technology developers. The Nursing Solutions Group is involved throughout the trial life cycle, from protocol development and feasibility analysis to clinical trial implementation and closeout. The Per Diem Mobile Research Nurse is a Registered Nurse who will work per diem and has experience across multiple therapeutic areas with the ability to work independently and integrate well with the Nursing Solutions Group. With interest/expertise in Science 37’s decentralized model of care delivery, the Mobile Research Nurse will perform delivery of care to participants as well as collaborate with brick and mortar sites, if indicated, for shared clinical trial implementation. The Mobile Research Nurse ensures the professional delivery of patient care in compliance with all federal and state regulations, Good Clinical Practice, and Standard Operating Procedures. *This is a travel role that requires on-site visits to participants homes. Duties for this position include but are not limited to: - Participate and provide research nurse services to qualified study participants at home - Apply clinical research and nursing practices to develop solutions to complex problems - Collaborate with Lead and Per Diem Mobile Research Nurses on solutioning, education, and resource support - Participate in activities that will further the operational development of Science 37 nursing service delivery - Develop relationships with study team members and serve as the subject matter expert (SME) on all nursing processes - Other duties as assigned as the needs of Science 37 evolve and change This position has the following qualifications: - BSN degree preferred - Full Covid Vaccination strongly preferred. Science 37 follows CDC guidelines for vaccination recommendations and such guidelines are subject to change. - Active RN licensure in home state as well as eligibility for Compact Licensure required - Minimum 2+ years clinical/research experience preferred - Basic Life Support (BLS) Certification - Maintain a positive reflection of the company by representation in participant’s homes or in clinic settings - Travel and availability qualifications are as follows: - 1-2 days minimum a week dedicated to support Science 37's study visits - Weekday/night availability required - Must be willing to travel to a participants homes - Active Driver’s License Science 37 is looking for people with the following skills and competencies: - BSN degree preferred - Active RN licensure in home state as well as eligibility for Compact Licensure required - Minimum 2+ years clinical/research experience preferred - Basic Life Support (BLS) Certification - Active Driver’s License - Weekday/night availability required - Maintain a positive reflection of the company by representation in participant’s homes or in clinic settings - Up to 100% travel, as needed, for study participant visits, project team meetings, and other professional meetings/conferences as needed - Ability to obtain nursing license in multiple states based on study needs - Physical ability to perform nursing tasks and lift equipment up to 15 kg in weight - Access to a reliable vehicle to perform study participant visits and transport equipment - Ability to drive to local and/or remote locations to perform study participant visits - Ability to use technology effectively and appropriately for study participant assessments and documentation including but not limited to study participant care equipment, laptop computers, communication devices and tablets - Ability to communicate in English (both verbal and written) There is minimal supervision for this position, with individuals reporting to the Manager, Nursing Solutions Group. Compensation varies based on location and work being performed. The starting pay range for a candidate selected for this position is generally within the range of $50-55 per hour. Employees may be eligible for additional discretionary bonuses and commissions. The successful candidate’s actual pay will also be based on qualifications and experience, so the actual starting pay may be above or below this range. Science 37 is an equal opportunity employer. We are committed to creating a diverse environment and is an equal opportunity employer. All qualified applicants receive consideration for employment without regard to age, race, ethnicity (including but not limited to hair texture and protected hairstyles), ancestry, color, sex, national origin, sexual orientation, gender, gender identity, gender expression, transgender status, religious creed, physical or mental disability (including actual or perceived disability), medical condition (including HIV/AIDS), pregnancy, perceived pregnancy and pregnancy related conditions, genetic information, marital status, political affiliation or activities, status as a victim of domestic violence, assault, or stalking, veteran status or participation in the uniformed military services of the United States, including the National Guard, or any other basis prohibited by applicable law. Science 37 values the well-being of its employees and aims to provide team members with everything they need to succeed. Submit your resume to apply! To learn about Science 37's privacy practices including compliance with applicable privacy laws, please click here
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Job Title: Clinical Trial Nurse – Per Diem Work Set‑Up: Local Travel – In‑Patient Home Are you a Registered Nurse interested in Clinical Trial work? IQVIA is seeking qualified Registered Nurses interested in community‑based and clinical trial work to visit patients in their homes. In this role, you will support clinical research by assisting with study visits, collecting data and samples, and helping evaluate the safety and efficacy of investigational medications. Visits and hours are flexible and can be arranged around your current work schedule; however, availability is required during morning to early afternoon hours. This role is ideal for PRN nurses or nurses currently working part‑time who are looking for supplemental income and professional growth. Key Responsibilities - Complete all reports and written assignments in a timely, accurate, and thorough manner, in accordance with established timelines and customer expectations. - Maintain a high level of professionalism in all interactions with patients, caregivers, and customer contacts. - Read, understand, and adhere to all applicable guidelines and regulations, including FDA regulations, fraud and abuse guidelines, pharmaceutical codes of conduct, HIPAA, and internal policies and procedures. Role of the Nurse During Home Visits Responsibilities may vary depending on the clinical trial but typically include: - Collecting required samples, information, and clinical data. - Obtaining vital signs, and conducting urine tests. - Administering investigational product (IP) via subcutaneous and/or intramuscular injection, as applicable. - Monitoring and assessing injection sites for reactions. - Reviewing adverse events (AE) and serious adverse events (SAE), and documenting findings per protocol. - Conducting concomitant medication reviews. - Performing urine pregnancy testing for women of childbearing potential (POCBP) at protocol‑specified timepoints (Weeks 28–36 and 40–50). - Labeling, packaging, and shipping of biological samples. - Reporting adverse events and protocol deviations as required. - Completing post‑visit documentation, reporting, and event notes accurately and promptly. Qualifications & Requirements - Active Registered Nurse (RN) license in home country (Argentina). - BLS certification required. - Experience or comfort with subcutaneous and intramuscular injections. - Ability to use basic computer and software applications for documentation and reporting. - Flexible availability and ability to accept assignments on short notice. - Willingness and ability to travel regionally by car, up to 90 miles, if required. - Must have a cellular phone, reliable transportation, and consistent internet access. - Ability to stand for extended periods; bending or kneeling may be required during visits. Why Join IQVIA? This per‑diem opportunity offers a flexible schedule, exposure to clinical research, and the chance to expand your professional experience while earning supplemental income. You will play a meaningful role in advancing healthcare and innovative therapies—directly from patients’ homes. Please note: This position is not eligible for sponsorship. Título del Puesto: Enfermero/a de Ensayos Clínicos – Per Diem Modalidad de Trabajo: Viajes Locales – Atención en el Domicilio del Paciente ¿Es usted Enfermero/a Profesional y le interesa trabajar en Ensayos Clínicos? IQVIA busca Enfermeros/as Profesionales calificados interesados en trabajo comunitario y en ensayos clínicos para realizar visitas a pacientes en sus hogares. En este rol, usted apoyará la investigación clínica asistiendo en visitas del estudio, recolectando datos y muestras, y contribuyendo a la evaluación de la seguridad y eficacia de medicamentos en investigación. Las visitas y los horarios son flexibles y pueden coordinarse según su disponibilidad actual; sin embargo, se requiere disponibilidad durante la mañana y primeras horas de la tarde. Este puesto es ideal para enfermeros/as PRN o profesionales que actualmente trabajen a tiempo parcial y busquen ingresos adicionales y desarrollo profesional. Responsabilidades Principales - Completar todos los informes y asignaciones escritas de manera oportuna, precisa y detallada, de acuerdo con los plazos establecidos y las expectativas del cliente. - Mantener un alto nivel de profesionalismo en todas las interacciones con pacientes, cuidadores y contactos del cliente. - Leer, comprender y cumplir con todas las normativas y lineamientos aplicables, incluidos los reglamentos de la FDA, políticas de fraude y abuso, códigos de conducta farmacéutica, HIPAA, y políticas y procedimientos internos. Rol del/de la Enfermero/a Durante las Visitas Domiciliarias Las responsabilidades pueden variar según el ensayo clínico, pero generalmente incluyen: - Recolección de muestras requeridas, información y datos clínicos. - Extracción de sangre, toma de signos vitales y realización de pruebas de orina. - Administración del producto en investigación (IP) mediante inyección subcutánea y/o intramuscular, según corresponda. - Monitoreo y evaluación de reacciones en el sitio de inyección. - Revisión de eventos adversos (AE) y eventos adversos graves (SAE), y documentación de los hallazgos conforme al protocolo. - Revisión de medicación concomitante. - Realización de pruebas de embarazo en orina para mujeres en edad fértil (POCBP), en los momentos especificados por el protocolo (Semanas 28–36 y 40–50). - Rotulado, embalaje y envío de muestras biológicas. - Reporte de eventos adversos y desviaciones del protocolo, según sea requerido. - Completar de forma precisa y oportuna la documentación posterior a la visita, informes y notas de eventos. Calificaciones y Requisitos - Licencia activa de Enfermero/a Profesional (RN) en el país de residencia (Argentina). - Certificación BLS vigente (obligatoria). - Experiencia comprobable en venopunción y extracción de sangre. - Experiencia o comodidad en la administración de inyecciones subcutáneas e intramusculares (deseable). - Capacidad para utilizar programas informáticos y software básicos para documentación y reportes. - Disponibilidad horaria flexible y capacidad para aceptar asignaciones con poco aviso. - Disposición y capacidad para viajar regionalmente en automóvil, hasta 90 millas, de ser necesario. - Contar con teléfono celular, transporte confiable y acceso constante a internet. - Capacidad para permanecer de pie por períodos prolongados; puede requerirse agacharse o arrodillarse durante las visitas. ¿Por Qué Unirse a IQVIA? Esta oportunidad per diem ofrece un horario flexible, exposición a la investigación clínica, y la posibilidad de ampliar su experiencia profesional mientras obtiene ingresos adicionales. Usted desempeñará un rol significativo en el avance de la atención médica y las terapias innovadoras, directamente desde el hogar de los pacientes. Nota: Este puesto no es elegible para patrocinio. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
• Assist with study management of assigned projects in accordance with SOPs, GCP, ICH guidelines and local regulations • Develop, organize and maintain tracking systems and tools across multiple programs • Coordinate and lead the development, review and maintenance of study management tools • Schedule meetings, coordinate and distribute meeting agendas, minutes, and follow-up action items • Establish, manage and oversee study files and shared spaces • Manage documentation of study training to ensure compliance • Develop collaborative relationships with vendor teams • Conduct and oversee quality control reviews of trial-level documents • Ensure timely, complete and compliant archiving of the TMF
Job Title Clinical Solution Specialist - Fetal Monitoring Job Description Bring your passion for patient care and technology to this role where you’ll be responsible for providing clinical customer support as the clinical application knowledge expert. You’ll facilitate solutions design, optimization, configuration, and delivery of Philips Fetal Monitoring products to ensure a quality customer experience. 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Clinical Solution Specialist - Patient Monitoring (Field: North Dakota/South Dakota)
PhilipsThere's always a way to make life better.
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