Clinical Research Nurse

Azza HealthCare Agency; Concord (MO); Sur place; USD 60 000 - 90 000; Plein temps

Résumé du poste

Azza HealthCare Agency is seeking a role to support and coordinate clinical trials in a Healthcare & Medical Services environment. The position focuses on managing study protocols and participant care while ensuring regulatory compliance and accurate data documentation.

The role requires strong nursing background, knowledge of informed consent processes, and a patient-centered approach to research participation.

Qualifications

• Strong nursing knowledge with experience supporting clinical research activities.
• Understanding of informed consent processes and regulatory requirements.
• High attention to detail for data collection, documentation, and compliance.
• Excellent communication and interpersonal skills for participant and team collaboration.
• Compassionate, patient-focused approach to research participation.

Responsabilités

• Manage and support study protocols and participant care within clinical trials.
• Ensure regulatory compliance and adherence to research and safety standards.
• Obtain informed consent and provide clear participant education.
• Collect, verify, and document clinical research data accurately.
• Deliver compassionate, patient-centered care throughout the research process.
• Collaborate with physicians, research coordinators, and multidisciplinary teams.

Connaissances

Nursing knowledge

Informed consent

Data collection

Communication skills

Patient-centered care

Description du poste

to support and coordinate clinical trials in a Healthcare & Medical Services environment.

Key Responsibilities

• Manage and support study protocols and participant care within clinical trials.
• Ensure regulatory compliance and adherence to research and safety standards.
• Obtain informed consent and provide clear participant education.
• Collect, verify, and document clinical research data accurately.
• Deliver compassionate, patient-centered care throughout the research process.
• Collaborate with physicians, research coordinators, and multidisciplinary teams.

Qualifications & Skills

• Strong nursing knowledge with experience supporting clinical research activities.
• Working understanding of informed consent processes and regulatory requirements.
• High attention to detail for data collection, documentation, and compliance.
• Excellent communication and interpersonal skills for participant and team collaboration.
• Compassionate, patient-focused approach to research participation.