63 clinical research coordinator jobs at 17 companies in Euless, TX
1mo
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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
3d
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Clinical Research Coordinator I
Dallas, Texas, United States
OnsiteFull Time
1+ YOEBachelor's degree in a medical or science-related field and one year of clinical research experience. Must coordinate studies, manage research data, interact with participants, and follow regulatory protocols.
Clinical trial management system, Electronic Medical Record, CRF
1mo
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Clinical Research Coordinator I
Dallas, Texas, United States
OnsiteFull Time
1+ YOEBachelor's in medical/science field, 1 year clinical research experience, familiarity with regulatory coordination, EMR and clinical trial management systems; BLS/CPR may be required; ACRP or SOCRA preferred.
Clinical Trial Management System, Electronic Medical Record
1w
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Clinical Research Coordinator
Dallas, Texas, United States
$23-$25/hr OnsiteFull Time
No clinical trial experience required; training provided. Requires independence, attention to detail, timely communication, interest in research, and comfort with direct patient contact.
PCR
2w
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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)
3mo
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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
3w
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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.
2w
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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
3w
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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.
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.
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.
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
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)
2mo
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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
5d
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Remote Clinical Research Data Coordinator II - Dallas, Tx
Dallas or Texas
RemoteFull Time
3+ YOEHigh school diploma required; associate or bachelor's degree preferred. Requires 3 years of medical office and data coordinator experience, clinical research knowledge, Microsoft Office, data entry, database management, and GCP/SOP knowledge.
Microsoft Office, USOR clinical trial management system, Microsoft HIPAA
1mo
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Research Coordinator
Dallas, Texas, United States
OnsiteFull Time
3+ YOEBachelor's degree required; 3 years clinical research experience preferred; knowledge of GCP and IRB processes; experience with REDCap, Epic, and Microsoft Office; CCRP preferred.
REDCap, Epic, Microsoft Office
1w
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Assistant Clinical Research Coordinator II
Dallas, Texas, United States
OnsiteFull Time
2+ YOEAccredited healthcare certification, certified medical assistant credential, CPR/BLS, 2+ years of clinical research, FDA/GCP, phlebotomy, and EKG experience; Microsoft Office proficiency required.
Microsoft Office Suite, Microsoft Excel, Microsoft Word, Microsoft PowerPoint, electronic data capture (EDC), EKGs
3d
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Research Coordinator
Irving or Fairfax or Houston
$43k-$108k/yr OnsiteFull Time
5+ YOETypically 5+ years of research or oncology care experience; current Texas or Virginia RN license for RNs, or a bachelor's degree for non-RNs. Oncology clinical trial and research coordination experience preferred.
electronic data capture, CRFs, IRB
1d
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Clinical Administrative Coordinator
Dallas or Hartford or Minneapolis or Phoenix or Tampa
$18-$32/hr RemoteFull Time
2+ YOEHigh school diploma/GED or equivalent experience, 2+ years in healthcare, medical claims processing or research, Microsoft Word, Outlook and Adobe PDF experience, and medical terminology familiarity.
Microsoft Word, Microsoft Outlook, Adobe PDF, ICD-10, CPT, UNET, CPA/Cosmos, CSP/Facets, Cirrus/USP, UHCW/NICE
2d
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Director of Study Operations
Fort Worth or Dallas
$135k-$145k/yr RemoteFull Time
Leadership experience overseeing clinical research operations, data coordination, medical records, staff training, compliance, study activation, process improvement, and patient care quality; master's degree and BLS/ACLS preferred.
Veeva, Clinical Trial Management System (CTMS), Electronic Health Record (EHR), Global Quality Management System (Global QMS)
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