50 clinical research coordinator jobs at 11 companies in Wake Forest, NC
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Clinical Research Coordinator
Durham, North Carolina, United States
$61k-$102k/yrOnsiteFull Time
Duke University: Private research university and academic health system.
Clinical research coordination experience, knowledge of GCP and human subject protections, strong organization and communication skills, and experience with research databases, EHRs, and study management systems.
University of North Carolina at Chapel Hill: The nation's first public university conducting innovative research and teaching.
1+ YOEBachelor’s degree in a related discipline plus one year of related training or experience, or equivalent combination. Pediatric clinical research and clinical trial coordination preferred.
Epic, OnCore, Veeva, Electronic Medical Records (EMR)
Cary or Michigan or Texas or Illinois or New Jersey or North Carolina or Detroit
OnsiteFull Time
Revival Research Institute: Independent U.S. clinical research site network conducting outpatient Phase I–IV trials for patients, physicians, and sponsors.
2+ YOERequires 2+ years coordinating industry-sponsored interventional trials at a research site, informed consent and monitoring experience, EDC proficiency, regulatory knowledge, and strong organizational and communication skills.
Electronic Data Capture (EDC), Microsoft Office, Microsoft Word, Microsoft Excel, Microsoft Outlook, ICH-GCP, FDA, 21 CFR Part 11, 21 CFR Part 50, 21 CFR Part 54, 21 CFR Part 56, 21 CFR Part 312, HIPAA, IATA, ECG, IRT, IWRS
Velocity Clinical Research: Clinical research site organization conducting Phase I–IV trials for pharma and biotech companies across U.S. and Europe.
4+ YOELead and manage clinical trials from startup through closeout per protocol, GCP/ICH and SOPs; mentor staff; perform clinical duties including phlebotomy and drug administration when in scope.
UTS- Temporary Clinical Research Coordinator at UNC Chapel Hill
Chapel Hill, North Carolina, United States
$31/hrHybridTemporary
North Carolina State University: Public research university and land-grant institution in North Carolina.
5+ YOEBachelor's degree and minimum 5 years clinical or human subjects research experience; skills in recruitment, regulatory compliance, data collection, GCP, project coordination, and communication; proficiency with Microsoft Outlook, Excel, and Word.
Microsoft Outlook, Microsoft Excel, Microsoft Word
Senior Clinical Research Associate (level dependent on experience)
Raleigh, North Carolina, United States
RemoteFull Time
CTI Clinical Trial and Consulting Services: Privately held global contract research organization serving pharmaceutical, biotechnology, and medical-device companies with clinical trials and consulting.
2+ YOESenior CRA coordinating site monitoring, enrollment strategies, visits, and regulatory docs; remote/home-based; requires allied health degree or RN with periphery nursing experience.
ProPharma Group: Private life-sciences consulting firm serving pharma, biotech, and medical-device companies with regulatory, clinical, and safety services.
3+ YOERequires 3+ years of data management experience and Electronic Data Capture experience; a bachelor's degree or allied health certification is preferred. Oracle Inform EDC, oncology, and inflammatory experience preferred.
Thermo Fisher ScientificNYSE: TMO: The world leader in serving science.
1+ YOE1+ (CTC I) to 2+ (CTC II) years clinical trial experience preferred, high school diploma (bachelor's preferred), knowledge of ICH GCP and SOPs, strong organizational and communication skills, MS Office proficiency.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint
Monitoring Excellence Academy - Oncology / CART/ Ophthalmology - CRA 1 - Central or West
United States or South Dakota or Michigan or Ohio or Illinois or California or Oklahoma or Utah or Missouri or Arizona or Idaho or Tennessee or Nevada or Washington or Oregon or Wisconsin or Montana or Texas or Colorado or Montreal or New Mexico or Indiana or Kansas or North Dakota or Durham
$80k-$90k/yrRemoteFull Time
FortreaNASDAQ: FTRE: Global contract research organization providing clinical development solutions.
University or college degree or allied health certification, 2+ years as a study coordinator or research nurse, and oncology, ophthalmology, or CAR T experience. Requires 60–70% overnight travel.
PSI CRO: Global full-service contract research organization providing clinical trial services.
4+ YOECollege degree in Life Sciences or equivalent, minimum 4 years CRO/clinical research experience, knowledge of ICH-GCP, TMF maintenance, strong communication, attention to detail, Microsoft Office proficiency, commutable to Durham, NC.