170 clinical trials regulatory coordinator jobs at 87 companies in United States
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Regulatory Coordinator - Sarcoma Clinical Trials
Boston or Brookline or Maine or Vermont or New Hampshire or Massachusetts or Connecticut or Rhode Island
$56k-$62k/yr RemoteFull Time
0+ YOEBachelor's degree or one year as an associate regulatory coordinator; strong communication, organization, computer, database, medical terminology, and basic clinical trial knowledge preferred.
Microsoft applications, databases, Food and Drug Administration (FDA), Institutional Review Board (IRB), Investigational New Drug (IND), Investigational Device Exemption (IDE)
3mo
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Clinical Trials Manager
Chicago, Illinois, United States
$60k-$85k/yr RemoteFull Time
2+ YOEManages and coordinates complex clinical trials; oversees protocol coordinators; ensures regulatory compliance and collaboration with study teams and external partners.
Regulatory Compliance, Clinical Trial Protocols, Project Coordination, Documentation, Stakeholder Communication
1mo
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Clinical Trials Regulatory Coordinator, Research Department, Kirk Kerkorian School of Medicine[R0152658]
Las Vegas, Nevada, United States
OnsiteFull Time
2+ YOEBachelor's degree and minimum 2 years clinical regulatory research experience; knowledge of IRB, GCP, FDA regulations; experience with clinical trial document preparation and maintenance.
2mo
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CLINICAL TRIALS SCREENING COORDINATOR I
United States
HybridFull Time
2+ YOEBachelor's degree in science/health/project management, 2 years clinical trials experience, patient-facing coordination or data/regulatory experience, strong communication and time-management skills, familiarity with regulatory requirements.
1mo
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Open Rank Clinical Trials Coordinator (Intermediate – Senior)
Aurora, Colorado, United States
$54k-$75k/yr OnsiteFull Time
2+ YOEOrganize and implement industry-sponsored clinical trial protocols, recruit and consent subjects, coordinate study procedures, manage regulatory submissions, perform phlebotomy and data entry.
Electronic Medical Records (EMR), Electronic Health Records (EHR)
1w
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Temporary Clinical Research Regulatory Coordinator
Orange, California, United States
$38/hr HybridFull Time, Temporary
Bachelor's degree or equivalent, 3–5 years of clinical research regulatory experience, and knowledge of FDA regulations, GCP, IRB processes, and Phase I–III trials. English proficiency required.
Electronic Medical Records (EMR), OnCore, Complion, Microsoft Excel
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Regulatory Coordinator
Gaithersburg, Maryland, United States
$27-$30/hr OnsiteFull Time
0+ YOERequires 0–2 years of clinical research regulatory experience, clinical trial and IRB knowledge, strong organization and communication skills, attention to detail, and proficiency in Microsoft Excel and Word.
Microsoft Excel, Microsoft Word
3mo
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Research Regulatory Coordinator
Springdale, Arkansas, United States
OnsiteFull Time
2+ YOERegulatory documentation and compliance for clinical trials; adherence to GCP; sponsor and IRB coordination; strong communication.
1w
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Regulatory Coordinator
Gaithersburg, Maryland, United States
$27-$30/hr OnsiteFull Time
0+ YOE0–2 years in clinical research regulatory affairs; knowledge of GCP, CFR, IRB processes, clinical trials, Excel and Word; strong organization, communication, critical thinking, and problem-solving skills.
Microsoft Excel, Microsoft Word, PC
1mo
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Clinical Research Coordinator III, Cardiac Clinical Trials
Los Angeles, California, United States
$71k-$92k/yr OnsiteFull Time
2+ YOEBachelor's in a related field plus 2+ years clinical research experience (or 5+ years without degree). Requires trial documentation, regulatory submissions, compliance knowledge, and BLS preferred.
3mo
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Clinical Research Coordinator III - Emergency Medicine Clinical Trials
Chicago, Illinois, United States
$29-$43/hr OnsiteFull Time
3+ YOEBachelor's degree or equivalent experience, 3+ years coordinating clinical trials, independent site management, regulatory knowledge (GCP/NIH/FDA/IRB), ability to manage multiple studies, travel readiness, and mentorship ability.
2mo
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Clinical Research Coordinator-Clinical Trials Management Office
Hilliard or Dublin or Powell or New Albany or Columbus
OnsiteFull Time
1+ YOEBachelor's in a related field (or equivalent), 1+ year clinical research experience, patient-facing coordination, informed consent, data collection, and familiarity with regulatory compliance.
Microsoft Software applications
1mo
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PS Regulatory Coordinator
Salt Lake City, Utah, United States
$39k-$61k/yr OnsiteFull Time
2+ YOEBachelor's degree in research or related field plus 2 years clinical trials/research experience (or equivalency). Patient-sensitive position requiring immunizations; regulatory experience and Microsoft Office skills preferred.
Microsoft Office, Microsoft Excel
1mo
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Regulatory Coordinator Assistant
Teaneck, New Jersey, United States
$27-$37/hr OnsiteFull Time
1+ YOEHigh school diploma required (associate preferred). Minimum 1 year clinical trials/regulatory/oncology experience. Knowledge of GCP, ICH, FDA, EMA. Strong attention to detail, multitasking, and communication skills.
eRegulatory systems, Clinical Trial Management Systems (CTMS), Electronic Data Capture (EDC), OncoEMR, Microsoft Word, PowerPoint, Microsoft Excel, PDF, Microsoft Teams, Zoom, Google Meet, internet applications
1mo
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UNIV - Regulatory Coordinator - Department of Medicine: Division of Pulmonary
Charleston, South Carolina, United States
$45k-$77k/yr OnsiteFull Time
1+ YOEBachelor's degree and 1 year relevant program experience; coordinating regulatory processes, IRB submissions, eSource and electronic regulatory binders, safety reporting, and administrative support for clinical trials.
3mo
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Clinical Research Coordinator
Omaha, Nebraska, United States
OnsiteFull Time
1+ YOECoordinate clinical research studies, ensure regulatory compliance, manage trial documentation, on-site with schedule Mon-Fri 8am-5pm.
EMR, Practice Management System
3mo
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Clinical Research Coordinator
Miami, Florida, United States
OnsiteFull Time
Coordinate and manage clinical trials; ensure regulatory compliance; recruit/enroll subjects; maintain study records; communicate with PI and Site Director.
Word, Excel, Study Manager
1mo
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Clinical Research Coordinator
Washington, District of Columbia, United States
$44k-$73k/yr OnsiteFull Time
2+ YOEManage and coordinate multiple clinical trials, conduct study visits, ensure protocol adherence, regulatory maintenance, timely data entry and adverse event reporting, and coordination with ancillary departments.
OnCore/CTMS
2mo
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Clinical Research Coordinator
Charleston, West Virginia, United States
OnsiteFull Time
2+ YOEManage site-level clinical trial operations, ensure regulatory compliance (GCP/SOP), coordinate patients and data entry to CTMS/EDC, maintain regulatory files, and support study documentation; 2 years site coordinating experience preferred.
FASMA Clinical Trial Management System (CTMS), EDC (Electronic Data Capture)
2mo
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Clinical Research Coordinator I
Bronx, New York, United States
$53k-$66k/yr OnsiteFull Time
BS required; CITI and OHS certifications; experience in clinical research/clinical trials preferred; responsible for consenting, data collection, regulatory submissions, specimen handling, and coordinating multi-department trial activities.
EDCs/Databases, imaging portals, Electronic Medical Record
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