Senior Clinical Research Coordinator — IRB & Study Ops

Cooper Norcross University Hospital; Camden (NJ); On-site; USD 40,000 - 66,000; Full time

Job summary

Cooper Norcross Health seeks a skilled research assistant to support the Principal Investigator and study team in protocol development, budget creation, and participant recruitment. You will help maintain accuracy of study documents and billing in EPIC, while adapting to evolving healthcare research workflows.

The role emphasizes collaboration with researchers and clinicians across departments to ensure compliant, efficient studies and high-quality data collection.

Qualifications

• Minimum 3-5 years of research experience required.
• High School Diploma or GED required.
• Bachelor's degree preferred.
• Basic understanding of Microsoft Excel, Outlook and Word.

Responsibilities

• Assist the Principal Investigator and research team with IRB protocol preparation and consent forms.
• Develop study budgets and maintain study documents.
• Assist with recruitment and identification of study participants as needed.
• Ensure proper research billing in EPIC and related systems.
• Complete and maintain all required study documentation.
• Adapt to evolving healthcare research environments and support team needs.
• Collaborate with team members and other departments on studies.

Skills

Attention to detail

Logical thinking

Team collaboration

Education

High School Diploma or GED

Bachelor's degree preferred

Tools

Microsoft Excel

Outlook

Word

Job description

Cooper Norcross Health seeks a skilled research assistant to support the Principal Investigator and study team in protocol development, budget creation, and participant recruitment. You will help maintain accuracy of study documents and billing in EPIC, while adapting to evolving healthcare research workflows.

The role emphasizes collaboration with researchers and clinicians across departments to ensure compliant, efficient studies and high-quality data collection.