Clinical Research Nurse II

Clinical Research Nurse

We are seeking a dedicated Clinical Research Nurse to join our team, where you will play a pivotal role in advancing clinical trials and research projects. Your expertise will be crucial in preparing IRB protocol submissions and informed consent forms, as well as identifying, recruiting, and interacting with patients throughout the study.

Responsibilities:

• Facilitate the 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:

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

Additional Skills & Qualifications:

• 5+ years of combined research and nursing experience
• Drug Trial Experience
• NJ-RN OR Compact License required.
• CRCC certification preferred.
• Advanced understanding of Microsoft Office.

Work Environment:

This position requires working fully on-site. As a part of our team, you will engage in a dynamic and collaborative environment, utilizing advanced technologies and equipment to support our clinical research efforts.

Job Type & Location:

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

Pay and Benefits:

The pay range for this position is $75000.00 - $120000.00/yr.

Workplace Type:

This is a fully onsite position in Camden, NJ.

Application Deadline:

This position is anticipated to close on Jun 5, 2026.