Oncology Clinical Trials Lead Nurse

University of Missouri System; Columbia Township (MO); Presencial; USD 75.000 - 100.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical insurance

Dental insurance

Vision insurance

Retirement plan

Paid time off

Disability benefits

Parental leave

Educational fee discounts

Descripción de la vacante

University of Missouri System, within the Medical Research Office at Ellis Fischel Cancer Center, seeks a Clinical Research Nurse to lead nursing management and coordination of oncology trials and participant care.

The role acts as the clinical and protocol expert, coordinating research activities across the participant's trial journey, ensuring safety, compliance, and high-quality data collection.

Formación

• Bachelor's degree in Nursing is required.
• Missouri RN license is required.
• Minimum of two years nursing experience in a hospital/clinic or similar setting is required.

Responsabilidades

• Screen, recruit, consent, enroll, and follow research participants per protocols and GCP.
• Coordinate protocol-required visits, assessments, treatments, and procedures with care teams.
• Monitor safety, adverse events, and report per regulatory requirements.
• Maintain source documents and support data collection, CRFs, monitoring, and audits.
• Participate in IRB/regulatory activities and ensure compliant submissions and reporting.
• Collaborate with regulatory and data staff to maintain accurate study records.
• Serve as clinical/operational expert for assigned oncology protocols and disease groups.
• Provide protocol-specific education to investigators and staff involved in study activities.
• Support study feasibility, sponsor visits, audits, and program development.
• Support enrollment goals and maintain participant safety and risk management.

Educación

Bachelor's degree in Nursing

Descripción del empleo

University of Missouri System, within the Medical Research Office at Ellis Fischel Cancer Center, seeks a Clinical Research Nurse to lead nursing management and coordination of oncology trials and participant care.

The role acts as the clinical and protocol expert, coordinating research activities across the participant's trial journey, ensuring safety, compliance, and high-quality data collection.