CLINICAL RESEARCH COORD II

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

About us

Cooper Norcross Health, formerly Cooper University Health Care, is a leading academic health system affiliated with Cooper Medical School of Rowan University. Headquartered in Camden, New Jersey, Cooper Norcross Health has revenues of more than $3 billion and an A+ credit rating from both S&P and Fitch Ratings.

Cooper Norcross Health has nearly 14,000 team members, including more than 2,200 nurses, more than 1,200 employed physicians representing 95 specialties and subspecialties, and more than 700 advanced practice providers.

The health system operates MD Anderson Cancer Center at Cooper as well as four hospitals – its 663-bed flagship Cooper Norcross University Hospital in Camden, its 229-bed Cooper Norcross University Hospital Cape Regional in Cape May Court House, Children’s Hospital at Cooper Norcross Health in Camden, and The Recovery Village Cherry Hill at Cooper, a substance abuse rehabilitation and inpatient treatment facility, in partnership with Advanced Recovery Systems.

Cooper Norcross University Hospital in Camden is the only Level 1 Trauma Center in South Jersey and the busiest in the region. The hospital has been recognized as a top-performing regional hospital by U.S. News & World Report’s Best Hospitals annual survey for eight years. More than 2.54 million patients visit Cooper Norcross Health facilities annually. Its ambulatory network encompasses three outpatient surgery centers, seven urgent care centers, a wound care center, and more than 130 physician, physical therapy, and radiology offices extending from the Delaware River to the New Jersey shore.

Cooper Norcross Health, a not-for-profit health system, was named one of America’s Best Large Employers for 2026 by Forbes, ranking among the top 200 in the nation. Visit CooperHealth.org(opens in new window) to learn more.

Short Description

Assists the Principal Investigator and other members of the research team 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 the changes healthcare is experiencing.

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.

Experience Required

Minimum 3-5 years of research experience required.

Education Requirements

High School Diploma or GED required

Bachelors Preferred

Special Requirements

Basic understanding of Microsoft Excel, Outlook and Word.