476 clinical trial coordinator jobs at 207 companies in United States
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Clinical Trial Coordinator
Orlando, Florida, United States
$55k-$70k/yr HybridFull Time
2+ YOE2-4 years in clinical trials, patient recruitment, pharmacy operations, or decentralized clinical programs; strong interpersonal and training skills; knowledge of IRB, HIPAA, and GCP; organized and proactive; proficient with CRM/clinical tracking systems.
CRM, Clinical Tracking Systems, Dashboards, Remote Collaboration Tools
2w
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Clinical Trial Coordinator - Martinsburg
Martinsburg, West Virginia, United States
OnsiteFull Time
3+ YOEBachelor's degree, minimum 3 years research experience, knowledge of clinical trial protocols, patient recruitment, regulatory compliance, and specimen collection; strong organizational and communication skills.
2mo
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Clinical Trial Screening Coordinator
Tomball, Texas, United States
OnsiteFull Time
3+ YOECoordinate pre-screening for clinical trials; ensure paperwork, eligibility, consent; knowledge of GCP/FDA; 3-4 yrs medical terminology; 1-2 yrs customer service; 1-2 yrs clinical research preferred.
CRIO, Electronic Medical Records, Microsoft Office
1w
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Clinical Trial Logistics Coordinator
Elmhurst or Richmond
$80k-$88k/yr HybridFull Time
2+ YOEHigh school diploma required; associate degree or equivalent preferred. Requires 2–4 years of clinical trial logistics, shipment coordination, customer communication, issue resolution, logistics knowledge, and strong computer skills.
Microsoft Office, order management systems, transportation management tools, customer portals, shipment tracking platforms
1w
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Clinical Trial Study Coordinator
Chico, California, United States
$27-$31/hr OnsiteFull Time
2+ YOEBachelor's preferred or 2+ years clinical research experience; HSP and GCP certification (or obtain within 5 business days); experience with clinical trial systems; strong communication and organizational skills.
Microsoft Office
2mo
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Clinical Trial Coordinator
Bethesda, Maryland, United States
HybridFull Time
Coordinate clinical trial activities, ensure FDA/IRB compliance, document procedures, train staff, and support NIH/NLM projects.
Electronic Lab Notebook, NIH systems, POTS
1w
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Principal Clinical Trial Coordinator - FSP
Wilmington or North Carolina
RemoteFull Time
5+ YOE5+ years relevant experience preferred, bachelor’s degree preferred, experience coordinating clinical projects, eTMF/Veeva familiarity, strong communication and regulatory knowledge.
Veeva, eTMF
2d
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Clinical Trial Leader
United States
RemoteFull Time
University degree in biomedical life sciences, strong international clinical trial project management experience, regulatory knowledge, scientific expertise, communication, leadership, coordination, and risk management skills.
Clinical Trial Management System (CTMS), Trial Master File (TMF)
1mo
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Clinical Trial Research Coordinator I
Houston, Texas, United States
OnsiteFull Time
2+ YOECoordinate day-to-day research protocol activities, screen and enroll patients, collect and enter clinical data, maintain study and regulatory records, follow ICH/GCP guidelines.
Clinical Trial Management System, Electronic Data Capture (EDC)
1d
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Clinical Trial Manager
San Carlos, California, United States
$129k-$218k/yr HybridFull Time
3+ YOERequires 3+ years of clinical trial operations experience in medical devices or diagnostics, multi-site study and CRO/vendor coordination, GCP/ICH knowledge, project management skills, and a relevant bachelor's degree.
da Vinci, Ion, Artificial Intelligence (AI)
1mo
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Clinical Trial Sample Manager
San Diego, California, United States
$145k-$169k/yr OnsiteFull Time
8+ YOEManage end-to-end clinical trial sample lifecycle with GCP compliance, cold-chain logistics, inventory reconciliation, and coordination with sites/CROs/labs; bachelor's degree and 8+ years in drug development required.
EDC
2w
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Clinical Trial Manager - Full Service
Morrisville, North Carolina, United States
OnsiteFull Time
Lead site management, clinical and central monitoring, ensure GCP/regulatory compliance, manage risks and budgets, coordinate cross-functional study activities, and supervise clinical monitoring staff.
Clinical Trial Management System (CTMS), Electronic Data Capture (EDC), eDiary, Electronic Patient Reported Outcomes (ePROs), Trial Master File (TMF), IVRS/IWRS, Central Monitoring dashboards
2mo
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Clinical Trial Project Manager
Cincinnati, Ohio, United States
HybridFull Time
1+ YOEBachelor's degree with 1+ year research experience, broad knowledge of medical terminology and clinical research methodology; project coordination and oversight skills.
2mo
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Senior Clinical Trial Associate - Oncology
Bedford, Massachusetts, United States
$108k-$132k/yr HybridFull Time
3+ YOE3+ years on phase I-IV clinical studies in biotech/CRO/academic settings; strong knowledge of ICH/GCP, TMF management, vendor oversight, audit support, and cross-functional coordination. BS/BA/RN (preferred).
Microsoft Project
3w
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Clinical Screening Coordinator
Rincon, Georgia, United States
OnsiteFull Time
Coordinating screening and assessment of participants for clinical trial studies at site level.
1mo
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CLINICAL RESEARCH COORDINATOR II
United States
HybridFull Time
2+ YOEBachelor's degree with 2 years clinical trials coordination experience (or associate's with 4 years); CCRP/CCRC preferred. Experience coordinating clinical trials, screening/enrolling subjects, and regulatory documentation.
1w
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Clinical Research Coordinator
Charlotte, North Carolina, United States
$25/hr OnsiteFull Time
2+ YOEManage clinical trials independently, ensure GCP/ICH/FDA compliance, perform participant coordination, clinical procedures, source documentation, and data management.
Rave, Inform, REDCap, CTMS, Microsoft Office
1mo
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Regulatory Coordinator II - Clinical Trial Office
Brookline or Maine or Vermont or New Hampshire or Massachusetts or Connecticut or Rhode Island
$61k-$68k/yr HybridFull Time
1+ YOECompletes regulatory submissions and tracking for clinical trials (IND/IDE, IRB, FDA), maintains regulatory files, coordinates study start-up, and ensures compliance with FDA and ICH/GCP; requires bachelor’s degree or equivalent experience and 1–3 years regulatory experience.
Microsoft applications, databases
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
3w
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Clinical Research Coordinator - Clinical Research
Savannah, Georgia, United States
$25-$29/hr OnsiteFull Time
Coordinate clinical trial activities per ICH/GCP and protocol; perform safety assessments, regulatory and administrative duties; communicate with sponsors and vendors; clinical research experience required.
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