Oncology Research Coord II PRN

About Us

Cooper Norcross Health formerly Cooper University Health Care is a leading academic health system affiliated with Cooper Norcross 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 14000 team members including more than 2200 nurses more than 1200 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 Childrens 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 American Recovery Services.

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 Reports 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 Americas Best Large Employers for 2026 by Forbes ranking among the top 200 in the nation. Visit to learn more.

Short Description

Oncology and Research are specialized and require unique skill sets. Realigning our MD Anderson Research Department at Cooper University Health Care with the MD Anderson Cancer Center at Houstons recommendation allows research growth in both the structure and the types of studies we are able to offer our clients to advance care. The role of the Oncology Research Coordinator I provides the oversight of clinical studies in the oncology setting managing Quality of Life and specimen trials while continuing to learn and advance in experience to manage oncology treatment trials. This is an entry level position.

Work with sponsors during the study start-up process to prepare the regulatory documents and maintain the studies regulatory binders throughout duration of study through close out including version control.

Work with the Institutional Review Board to submit initial study applications amendments continuing reviews adverse event reports and other submissions.

Provide regular updates to the Regulatory and Operations team members on where studies are in the review/start-up process monitoring outcomes and close out preparation.

Maintain the delegation of authority logs and regulatory documentation for each study and ensure study staff training on each protocol.

Work with sponsors to set up site initiation visits monitoring visits and study close-out visits and prepare post-visit documents.

Maintains tracking for all protocol related paperwork and collects documents from sponsors for protocol submission and maintenance.
Coordinates FDA submissions and prepares for all research audits.

Experience Required

3-5 Related experience

Education Requirements

Bachelor Degree Preferred

Salary Min ($)

USD $31.00

Salary Max ($)

USD $53.00