142 research coordinator jobs at 62 companies in North Carolina
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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.
Boston or United States or United Kingdom or Canada or London or Oakland or Burlington or Nahant or Arlington or Charlotte or Miami or Portland or Seattle or Toronto or Vancouver or Africa
$49k-$67k/yrOnsiteFull Time
Northeastern University: Global research university offering experiential learning and degree programs.
Bachelor’s degree in psychology, neuroscience, public health, or related field; organizational and communication skills, independent work, and large-scale pediatric or clinical trial data experience required.
Innovo Research: Provides integrated clinical research services across healthcare networks.
1+ YOEBachelor's degree,1+ years clinical research experience,proficiency with Microsoft Office,knowledge of GCP/ICH and FDA regs,clinical skills (phlebotomy,vital signs),strong communication and organizational skills.
Novant Health: Operates an integrated network of hospitals and medical clinics.
5+ YOEHigh school diploma required (bachelor's preferred). Minimum 5 years clinical research experience (degree substitutions allowed). Research certification (ACRP/SOCRA) preferred. Strong clinical research knowledge, communication, database and time-management skills.
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)
Odyssey Systems: Provides engineering, integration, and technical services to defense clients.
3+ YOEUS citizen with ability to obtain Secret clearance, bachelor's degree in biology/psychology/related field (master's preferred), 3+ years clinical investigations experience, human subjects training, CCRC/CCRP/CCRA preferred, Microsoft Office proficiency.
High Point University: Private university providing undergraduate and graduate academic programs.
3+ YOEUndergraduate degree and 3+ years of database management or institutional research experience. Requires relational databases, Excel, research, confidentiality, communication, prioritization, detail, and teamwork skills.
Microsoft Office, Microsoft Excel, Raiser’s Edge, Raiser’s Edge NXT, Power BI, Power Automate, Target Analytics, Internet
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)
Odyssey Systems: Provides technical engineering and program management for government agencies.
3+ YOEUS citizen with ability to obtain Secret clearance; bachelor’s degree in biology/psychology/related field required (master’s preferred); 3+ years clinical investigations experience; CCRC/CCRP/CCRA preferred; human subjects training; Microsoft Office proficiency.
OrthoCarolina: Provides specialized medical care for bones, joints, and muscles.
Bachelor's degree required. CCRC preferred. Requires strong organization, communication, deadline management, problem-solving, medical terminology, and proficiency with word processing, spreadsheets, and electronic data capture systems.
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)
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
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.
3+ YOE3+ years CRC experience, recent phlebotomy experience, familiarity with GCP and federal regulations, bachelor’s degree preferred, strong documentation and communication skills.
IVR systems, electronic data capture, clinical trials database, Microsoft Word, Microsoft Excel, EDC
Clinical Research Coordinator II- Murtha Cancer Center
Fort Bragg or Bethesda
$61k-$80k/yrOnsiteFull Time
The Henry M. Jackson Foundation for the Advancement of Military Medicine: Administers and supports military medical research programs.
3+ YOEBachelor's degree, minimum 3 years clinical research experience, U.S. citizenship, experience consenting patients and processing/shipping blood samples preferred, regulatory/IRB and oncology experience preferred, complete CITI human protections training within one month.
SiteBridge Research: Operates a national network of community-based clinical research sites.
3+ YOEBachelor's in life sciences, 3+ years clinical site/trials experience, knowledge of FDA & ICH GCP, detail-oriented, strong communication and analytical skills, Microsoft Office proficiency; willingness to travel up to 25%.