3w
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Clinical Research Coordinator
Farmers Branch, Texas, United States
OnsiteFull Time
1+ YOEManage day-to-day clinical trial operations, recruit and engage participants, ensure GCP/FDA/HIPAA compliance, document data, and coordinate with sponsors; 1-2 years clinical research experience preferred.
Microsoft Office, Clinical Research IO (CRIO), CTMS
2mo
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Senior Clinical Research Coordinator
Dallas, Texas, United States
OnsiteFull Time
4+ YOEClinical research team leader role requiring clinical research coordinator experience (4–8 years depending on education), CCRC certification (ACRP/SOCRA) within 6 months, phlebotomy/IV/IM credentials as applicable, and advanced clinical, communication, and leadership skills.
Microsoft Office
1w
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Clinical Research Coordinator II
Dallas, Texas, United States
OnsiteFull Time
2+ YOEBachelor's in medical/science, 2 years clinical research experience, BLS/CPR/AED may be required, ACRP or SOCRA preferred; experience with regulatory documentation and patient coordination.
electronic medical record, clinical trial management system, telehealth
6d
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Clinical Research Coordinator I
Richardson, Texas, United States
OnsiteFull Time
2+ YOEAssociate degree or HS+2 years relevant experience; basic clinical research knowledge; ability to coordinate studies, manage documentation, and use EDC; strong communication and multitasking skills.
Electronic Data Capture (EDC)
2mo
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Senior Clinical Research Coordinator
Dallas, Texas, United States
OnsiteFull Time
4+ YOEBachelor's +4yrs or Associate+6yrs or High School+8yrs clinical research coordinator experience; CCRC within 6 months, phlebotomy/IV administration as required, advanced communication and organizational skills.
Microsoft Office
4d
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Clinical Research Coordinator I
Dallas, Texas, United States
OnsiteFull Time
1+ YOEBachelor's in medical or science field,1 year clinical research experience, BLS/CPR (may be required),ACRP/SOCRA a plus,ability to coordinate participants,manage regulatory documents,and use EMR and trial systems.
Electronic Medical Record (EMR), Clinical trial management system
2w
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Research Coordinator, Sports Medicine
Frisco, Texas, United States
OnsiteFull Time
3+ YOEBachelor's degree, experience in clinical research (3+ years preferred), CCRP preferred, EMR experience (EPIC) and Microsoft Office proficiency, strong communication and organizational skills.
Microsoft Office, EPIC
1w
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Clinical Research Coordinator II
Amarillo or Dallas
OnsiteFull Time
3+ YOE3+ years clinical research coordination experience; patient-facing skills including consenting, assessments, blood draws, medication administration, ECG, regulatory compliance, clean data entry; legal US work authorization required.
1mo
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Clinical Research Coordinator
Fort Worth, Texas, United States
OnsiteFull Time
2+ YOEHigh School diploma/GED, 2 years clinical research experience, working knowledge of GCP and oncology Phase 1 trials, strong communication and organizational skills, proficiency with Microsoft Office and clinical trial management software.
Microsoft Office Suite, clinical trial management software
5d
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Clinical Research Coordinator II
Plano, Texas, United States
OnsiteFull Time
3+ YOEAssociate's or Bachelor's in a scientific/healthcare field, 3+ years clinical research or healthcare experience, CTMS/EDC proficiency, research certification preferred (CCRC/CCRP), ability to perform clinical procedures and maintain regulatory documentation.
CTMS, EDC
2w
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Clinical Research Coordinator II
Dallas, Texas, United States
$23-$28/hr OnsiteFull Time
1+ YOEBachelor's degree, minimum 1 year clinical research experience with industry-sponsored trials, ability to manage complex studies, strong communication and sponsor-facing skills.
3mo
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Dallas Clinical Research Project Coordinator
Irving, Texas, United States
OnsiteFull Time
Bachelor's degree in life sciences required; strong computer, organizational and time-management skills; research experience preferred; 4-6 week training program provided for project coordinators.
3mo
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Research Coordinator 2
Dallas, Texas, United States
OnsiteFull Time
2+ YOEBachelor degree or Medical Assistant; RN preferred; Medical Assistant Certification or CCRC required; LVN/RN license preferred; 2+ years related experience.
1mo
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Dallas Clinical Research Project Coordinator
Irving, Texas, United States
OnsiteFull Time
Bachelor's in life sciences, strong computer, organizational and time-management skills; research experience preferred; 4-6 week training provided for those without clinical research experience.
2w
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Research Data Coordinator - Dallas, Tx
Dallas, Texas, United States
OnsiteFull Time
High school diploma required (associate/bachelor preferred). Entry-level to senior tiers: 0–7+ years medical office/data coordinator experience; SoCRA/ACRP preferred; medical terminology and oncology experience preferred.
1w
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Clinical Research Coordinator
Dallas, Texas, United States
OnsiteFull Time, Temporary
Supports coordination of clinical studies, participant screening and consent, data collection, regulatory compliance, specimen handling, and study documentation. High school diploma required; associate in health-related field preferred.
electronic data capture systems, clinical trial management software, Microsoft Excel, Microsoft Word, Microsoft PowerPoint
2mo
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Clinical Research Coordinator I
Dallas, Texas, United States
OnsiteFull Time
1+ YOEHigh school diploma required; Bachelor’s preferred; 1 year CRA/Coordinator experience; 1-2 years in clinical research; bilingual English/Spanish; proficient in CRIO/CTMS and MS Office; GCP/ICh knowledge; BLS; valid driver’s license.
Microsoft Office, CRIO, Clinical Trial Management System (CTMS)
1mo
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Clinical Research Coordinator II (3763)
Irving, Texas, United States
OnsiteFull Time
2+ YOEHigh school diploma required (bachelor's preferred); 2+ years CRC experience preferred; ICH-GCP and IATA training; ACRP preferred; proficiency in English (Spanish preferred); experience with EDC/IVRS and clinical documentation.
EDC, IVRS
2mo
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Clinical Research Coordinator
Irving, Texas, United States
OnsiteFull Time
1+ YOEBachelor’s degree in life sciences; 1-2 years clinical industry experience; GCP knowledge; human protections; computer skills.
Microsoft Office, Electronic Data Capture
3w
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Postdoctoral Research Associate
Bryan or Austin or Dallas or El Paso or Fort Worth or Houston or Laredo or San Antonio
HybridFull Time
PhD in relevant field; strong quantitative skills with statistical programming (R or Python), causal inference, spatial analysis, stakeholder engagement, and project coordination for multi-country research.
R, Python, SHERPA, SHERPA-City, ArcGIS, QGIS
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