ONCOLOGY RESEARCH COORD II PRN

Cooper University Health Care

Camden (NJ)

On-site

USD 43,000 - 73,000

Full time

14 days+

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Job summary

Cooper Norcross Health is seeking an Oncology Research Coordinator II PRN to oversee clinical studies in the oncology setting, focusing on Quality of Life and specimen trials while advancing in experience to manage oncology treatment studies.

This entry-level role supports start-up activities, IRB submissions, regulatory documentation, sponsor communications, and site visits, with day shifts in Camden, NJ and per diem compensation.

Qualifications

  • 3-5 related experience.

Responsibilities

  • Oversee clinical studies in oncology, including QoL and specimen trials.
  • Coordinate regulatory documents and study binders throughout the study duration.
  • Submit IRB applications, amendments, continuing reviews, and adverse event reports.
  • Maintain delegation of authority logs and ensure staff training on each protocol.
  • Coordinate sponsor visits and prepare post-visit documents.
  • Prepare FDA submissions and audit readiness.

Education

Bachelor Degree Preferred

Job description

ONCOLOGY RESEARCH COORD II PRN

Location: Camden, NJ

Job ID: 73150

Job Type: Per Diem

Shift: Day

Specialty: Other Professional

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 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 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 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

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 Houston's 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

Hourly Rate Min $31

Hourly Rate Max $53

The New Jersey Pay Transparency Act requires disclosure of the pay range for this position.

A salary offer will vary based on the job role, candidate experience, qualifications, internal pay equity and market data.

Cooper University Health Care is an Equal Opportunity Employer and is committed to equal employment opportunity for all team members. All employment decisions are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, or any other status protected by law or regulation. To request reasonable accommodation, contact talent-acquisition@cooperhealth.edu

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