Clinical Research Nurse I

Clinical Research Nurse

The Clinical Research Nurse I plays a vital role in facilitating the preparation of IRB protocol submissions and informed consent forms. This position is key in identifying, recruiting, and interacting with patients throughout the entire study. You will be responsible for completing and maintaining all study documents in compliance with Health System, sponsor, and FDA requirements.

Responsibilities

• Facilitate preparation of IRB protocol submissions and informed consent forms.
• Identify, recruit, and interact with patients throughout the entire study.
• Complete and maintain all study documents in compliance with Health System, sponsor, and FDA requirements.

Essential Skills

• Proficiency in clinical research and clinical trial processes.
• Experience with regulatory and data management procedures.
• Skills in patient recruitment and IRB protocol management.
• Familiarity with Epic and EDC systems.
• Knowledge of drug or device trials, especially in neurology.
• Understanding of Good Clinical Practice (GCP) guidelines.

Additional Skills & Qualifications

• Graduate from an accredited RN program.
• Possession of a NJ-RN License.
• Advanced understanding of Microsoft Office.
• Certification as a Clinical Research Coordinator (CRCC) preferred.

Work Environment

This position is fully onsite, offering an engaging and collaborative environment. You will be working with advanced technologies and equipment related to clinical research and trials. The facility maintains a professional atmosphere with a focus on compliance and patient-centered care.

Job Type & Location

This is a Permanent position based out of Camden, NJ.

Pay and Benefits

The pay range for this position is $70000.00 - $93600.00/yr.

Workplace Type

This is a fully onsite position in Camden, NJ.

Application Deadline

This position is anticipated to close on May 30, 2026.