Clinical Research Coordinator II — IRB, Budgeting & EPIC

Cooper University Health Care; Camden (NJ); On-site; USD 52,000 - 72,000; Full time

Job summary

Cooper Norcross Health in Camden, NJ seeks a Research Coordinator to support the Principal Investigator and research team with IRB protocol preparation, consent forms, and study budget development. You will help ensure accurate documentation and compliance for clinical studies conducted within the system.

The role supports project tasks, maintains study records, recruits participants, and collaborates across departments.

Qualifications

• Minimum 3–5 years of research experience.
• Assist with IRB protocols, consent forms, and study budgets.
• Ensure proper research documentation and billing in EPIC.

Responsibilities

• Assists the Principal Investigator and other team members with preparation of IRB protocols, consent forms, and development of study budget.
• Completes and maintains all study documents as required.
• Assists with projects as needed or assigned.
• Ensures proper research billing in EPIC.
• Is flexible and can adapt to changes in healthcare.
• Assists with the identification and recruitment of study participants.
• Work as a team player with all involved in the studies.
• Additional duties as assigned by manager.

Skills

Research experience

Team player

Adaptability

Education

High School Diploma or GED

Bachelor's preferred

Tools

EPIC

Excel

Outlook

Word

Job description

Cooper Norcross Health in Camden, NJ seeks a Research Coordinator to support the Principal Investigator and research team with IRB protocol preparation, consent forms, and study budget development. You will help ensure accurate documentation and compliance for clinical studies conducted within the system.

The role supports project tasks, maintains study records, recruits participants, and collaborates across departments.