Clinical Research Regulatory Coordinator - CNI
$31 per hourCooper University Health Care
About UsCooper 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 DescriptionThe 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 Required3-5 years required. Education RequirementsBachelor’s Degree required. Masters preferred. Salary Min ($)USD $31.00Salary Max ($)USD $53.00Job SummaryJob ID: 67600Category: ProfessionalsShift: 1Type: Full TimeDepartment Name: Administration CNI 101 Haddon Ave
$62k - $67.79k
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...approach powers pioneering research and development advancements... ...GSL) leads global Phase I–IV clinical trials, overseeing strategy,... ...archiving in compliance with regulatory and company requirements. \n... ...and inspections. \n Coordinate Investigational Medicinal Product...RegulatoryWork at officeWorldwideFlexible hours- ...Positions In Requisition 1 Job Details A full-time Clinical Research Coordinator position is available in the Lung Cancer Screening and... ...overall to patients. Assists Principal Investigator with regulatory body filings, including IRB submissions. May assist in...RegulatoryDaily paidFull timeTemporary workPart timeFlexible hoursShift work
- ...the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP). Runs portions of... ...to closeout including protocol coordination (screening recruiting enrolling... ...for monitoring visits and regulatory and/or IRB document preparation...RegulatoryDaily paidFull timeTemporary workPart timeWork at officeRemote workFlexible hoursShift work
$47.31k - $53.42k
...world-renowned leader in education, research, and innovation. This historic, Ivy... ...and much more. Posted Job Title Clinical Research Coordinator A/B (OBGYN - Pregnancy & Perinatal... ...biospecimens, subject visits and follow-up and regulatory documentation. Job...RegulatoryFull timeLocal areaWork from homeFlexible hours- CenExel is seeking a Clinical Research Coordinator I to coordinate all aspects of clinical trials with strict adherence to ICH, GCP, and protocol... ...leadership, and problem-solving skills, with a focus on regulatory compliance, data integrity, and efficient study #J-18808...Regulatory
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- ...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...RegulatoryFull timeShift work
$26.09 - $33.32 per hour
About Us: Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence... ...Responsible for assisting with coordinating clinical trials with the strictest... .... Performs administrative and regulatory duties related to the study as...RegulatoryFull timeWork at officeShift workNight shift$53k - $66.3k
...'s HBCD team is looking to expand with the addition of a Clinical Research Coordinator I. In this full-time role, the CRC-I will be responsible... ...events Understand good clinical practice (GCP) and regulatory compliance Educate subjects and family on protocol, study...RegulatoryFull timePart timeFor contractorsShift work- ...supervision and oversees the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP). Performs a variety of research... ...patients. Assists Principal Investigator with regulatory body filings including IRB submissions. May...RegulatoryDaily paidFull timeTemporary workPart timeFlexible hoursShift work
$50k - $55k
...Pulm/CriticalCare/SleepMed Department is searching for a Clinical Research Coordinator! Become a part of the Temple family and you will have... ...clinical trials, ensuring high-quality data collection, regulatory compliance, and seamless study operations. As a Clinical...RegulatoryFull timeWeekend workAfternoon shift- ...supervision and oversees the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP). Performs a variety of research... ...patients. Assists Principal Investigator with regulatory body filings including IRB submissions. May...RegulatoryDaily paidFull timeTemporary workPart timeFlexible hoursShift work
- ...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
$7.25 - $22.36 per hour
...Clinical Research Coordinator - Temporary The University of Pennsylvania, the largest private employer in Philadelphia, is a world-renowned leader in education, research, and innovation. This historic, Ivy League school consistently ranks among the top 10 universities...Hourly payTemporary workLocal areaWork from home$47.31k - $50k
...Clinical Research Coordinator As part of the Department of Psychiatry, Neurodevelopment and Psychosis Division, the Penn Psychosis Evaluation and Recovery Center (PERC) offers consultations on diagnosis, treatment, support and skill development for adolescents and young...Local areaShift work- ...Number of Positions In Requisition 1 Job Details Clinical Research Coordinator- PKPD Job Description Works under limited supervision and oversees the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP). Performs...Daily paidFull timeTemporary workPart timeFlexible hoursShift workAfternoon shift
$25 - $36 per hour
...Job Description Job Description About Us Flourish Research is where clinical trials thrive. Flourish Research is one of the industry’s... ...the Job: We are actively hiring a Clinical Research Coordinator to support our Philadelphia site. Shift: Monday-Friday...Hourly payWork at officeMonday to FridayShift work- ...Securities Industry Oversight (FSIO). As an Assistant Director, you will join a well-respected team that is responsible for supporting EXAMS' mission to conduct and coordinate the examination program for certain SROs over which the Commission has regulatory authority....RegulatoryWork at office
$20 per hour
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- ...a well-respected team that is responsible for supporting EXAMS' mission to conduct and coordinate the examination program for certain SROs over which the Commission has regulatory authority. In this role as an Assistant Director, you will be responsible for: Planning...RegulatoryLocal area
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$225k - $255k
...including annuity, health, life, long-term care, disability, and property & casualty. Our practice also covers a broad array of regulatory, compliance, and transactional matters, including with respect to corporate governance, insurance holding company regulation, investment...RegulatoryImmediate start$120k - $210k
...a visionary scientific strategist capable of turning complex clinical data into impactful Medical Affairs communication plans?We are... ...foundational understanding of Medical Affairs compliance and regulatory guidelines.What We OfferCompetitive salary and comprehensive benefits...Regulatory
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