Clinical Research Regulatory Coordinator - CNI
$31 per hourCooper Norcross University Hospital
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 to learn more.
Short Description
- The Clinical Research Regulatory Coordinator ensures regulatory compliance and accurate documentation for all clinical research studies conducted at Cooper University Health Care.
- This role supports study startup, maintenance, and closeout by managing submissions to regulatory agencies, maintaining Investigator and staff documentation, and facilitating communication among Investigators, sponsors, and institutional offices.
Experience Required
3-5 years required.
Education Requirements
Bachelor's Degree required. Masters preferred.
Salary Min ($)
USD $31.00
Salary Max ($)
USD $53.00
$31 per hour
...Visit CooperHealth.org to learn more.Short DescriptionThe Clinical Research Regulatory Coordinator ensures regulatory compliance and accurate documentation... ...SummaryJob ID: 67600Category: ProfessionalsShift: 1Type: Full TimeDepartment Name: Administration CNI 101 Haddon AveRegulatoryCooper University Health Care
Camden, NJ8 hours ago- ...Clinical Trial Coordinator Works under limited supervision and oversees the day-to-day activities... ...trial in accordance with Good Clinical Research Practice (GCP). Performs a variety of... ...Assists Principal Investigator with regulatory body filings including IRB submissions...RegulatoryTemporary workPart timeShift work
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Shriners Children's Chicago
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...Clinical Research Coordinator A/B/C The Clinical Research Coordinator A/B/C will support the coordination and execution of clinical research... ...complexity. Responsibilities include study coordination, regulatory support, subject recruitment and enrollment, study visits...RegulatoryLocal areaFlexible hoursThe University of Pennsylvania
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Philadelphia, PA1 day ago$47.31k - $70k
...world-renowned leader in education, research, and innovation. This historic, Ivy... ...and much more. Posted Job Title Clinical Research Coordinator A/B/C Job Profile Title... ...recruitment and enrollment, study visits and regulatory compliance in one or more studies. Our...RegulatoryFull timeLocal areaWork from homeFlexible hoursUniversity of Pennsylvania
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Thomas Jefferson University
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$47.31k - $53.42k
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...the 'how' and transforming clinical trials through better integration... ...engineering, technology and regulatory, and with people who share... ...the future of clinical research and improve patients' lives... ...Certified Clinical Research Coordinator, Associate or Professional (...RegulatoryFull timeFor contractorsLocal areaVisa sponsorshipWork visaFlexible hoursN-Power Medicine
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- ...the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP). Runs portions of... ...closeout, including protocol coordination (screening, recruiting, enrolling... ...for monitoring visits, and regulatory and/or IRB document preparation...RegulatoryDaily paidFull timeTemporary workPart timeFlexible hoursShift work
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