55 clinical research coordinator jobs at 12 companies in Durham, NC
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Clinical Research Coordinator
Durham, North Carolina, United States
$61k-$102k/yrOnsiteFull Time
Duke Health: Provides comprehensive medical care, clinical research, and health education.
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: Public research university offering undergraduate and graduate degree programs.
Bachelor’s degree or equivalent training and experience; knowledge of clinical research, GCP, FDA regulations, IRB processes, medical terminology, and strong written and verbal communication skills.
Microsoft Outlook, Microsoft Excel, Microsoft Word, Good Clinical Practice (GCP), Institutional Review Board (IRB)
IQVIANYSE: IQV: Provides clinical research and healthcare data analytics services.
1+ YOEMinimum 1 year CRC clinical research experience, working knowledge of GCP and clinical trial processes, ability to perform study procedures and accurate EDC data entry, strong organizational and interpersonal skills.
CRIO (Clinical Research IO), Electronic Data Capture (EDC)
IQVIANYSE: IQV: Provides clinical research and data analytics for pharmaceutical companies.
1+ YOE1+ year clinical research experience, knowledge of GCP, ability to perform study procedures, EDC data entry, regulatory documentation, patient interaction, and strong organizational skills.
Electronic Data Capture (EDC), Clinical Research IO (CRIO)
Velocity Clinical Research: Operates a global network of integrated clinical research sites.
1+ YOEConduct and manage clinical trials per protocol and GCP; regulatory document preparation, subject recruitment, data entry, adverse event reporting, phlebotomy and clinical task performance as required.
Care Access: Conducts decentralized clinical trials and community health screenings.
1+ YOEMinimum 1 year CRC experience, recent phlebotomy experience, knowledge of GCP/ICH/FDA, ability to follow SOPs, strong organizational and communication skills, experience with clinical databases/IVR/EDC/MS Word and Excel.
e-source, Electronic Data Capture, IVR systems, clinical trials database, MS Word, Microsoft Excel
UTS- Temporary Clinical Research Coordinator at UNC Chapel Hill
Chapel Hill, North Carolina, United States
$31/hrHybridTemporary
North Carolina State University: Public research university offering undergraduate and graduate degree programs.
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
CTI Clinical Trial and Consulting Services: Clinical trial management and consulting for life sciences companies.
1+ YOEBachelor's in allied health or equivalent experience, at least 1 year clinical research experience, ability to support project management, prepare clinical documents, and maintain project tracking.
Senior Clinical Research Associate (level dependent on experience)
Raleigh, North Carolina, United States
RemoteFull Time
CTI Clinical Trial and Consulting Services: Global healthcare research organization providing remote opportunities and dedicated training.
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: Provides clinical, regulatory, and compliance services to life sciences.
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: Sells equipment and chemicals for scientific research and healthcare.
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
Syneos Health: Global biopharmaceutical services for clinical development and commercialization.
1+ YOERN or bachelor’s degree required, 1+ year clinical research experience (2+ preferred), clinical research certification preferred, GCP knowledge, proficient with Word/Excel/PowerPoint and EDC/Medidata.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Medidata
PSI CRO: Manages clinical trials for the pharmaceutical and biotechnology industries.
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.
ICONNASDAQ: ICLR: Provides outsourced clinical research and drug development services.
3+ YOERequires 3–5 years in clinical research, operations, patient engagement, project management, or related work, plus vendor coordination, descriptive analysis, Excel, presentation tools, and ICH-GCP and privacy knowledge.