1,100 clinical data coordinator jobs at 416 companies in United States
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Clinical Data Coordinator
Austin, Texas, United States
OnsiteFull Time
Thermo Fisher ScientificNYSE: TMO: The world leader in serving science.
0+ YOEBachelor's degree or equivalent and 0–2 years of relevant experience. Requires clinical terminology knowledge, analytical skills, attention to detail, communication, confidentiality, and regulatory and SOP compliance.
The Start: Private early-phase oncology clinical research network serving cancer patients, physicians, and biopharma sponsors.
Collect, enter, review, and transmit clinical study data (paper and electronic CRFs); coordinate monitor visits; bachelor’s degree or equivalent experience and experience in a clinical research organization required; CCRP or CCRC preferred.
Madrigal PharmaceuticalsNASDAQ Global Market: MDGL: Public biopharmaceutical developing and commercializing treatments for MASH patients with serious liver disease.
1+ YOEBachelor's in life sciences or computer science; 1–2 years clinical data management or related experience; knowledge of GCP/ICH/FDA; experience with EDCs and MS Office; attention to detail and communication skills.
Medidata Rave, Oracle InForm, Veeva CDMS, Microsoft Excel, Microsoft Word, Microsoft PowerPoint, Microsoft Outlook
MedpaceNASDAQ: MEDP: Global full-service clinical contract research organization.
PharmD or PhD required; bachelor’s in life science noted; strong attention to detail, communication, Excel and Word proficiency; experience with research/statistical data preferred.
MedpaceNASDAQ: MEDP: Global full-service clinical contract research organization.
PharmD or PhD required; bachelor's in life science preferred. Experience with research/statistical data preferred. Strong attention to detail, communication skills, multitasking ability, and proficiency with Excel and Word.
Clinical Data Coordinator (Clinical Research Technician)
Indianapolis, Indiana, United States
OnsiteFull Time
Indiana University Indianapolis: Public research university system headquartered in Indiana.
1+ YOESupports conduct of clinical research including subject recruitment, consenting, data collection, specimen handling, documentation, and regulatory record keeping. Requires patient-related or research experience and relevant post-secondary education.
EDETEK: Clinical CRO and software provider serving pharmaceutical, biotech, and medical-device companies.
Ensures accuracy and reliability of clinical trial data through validation, reconciliation, reporting, coordination with study teams, and quality improvement.
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.
Hackensack University Medical Center: Nonprofit academic medical center providing adult and pediatric care, research, and medical education to New Jersey communities.
4+ YOEBA/BS in science or healthcare, or 4+ years related experience with high school diploma/GED. Requires data management, research documentation, computer proficiency, communication, organization, and deadline management.
Microsoft Office, Google Suite, Case Report Form (CRF)
Yale School of Medicine: Ivy League research university in New Haven, Connecticut.
2+ YOEBachelor's degree in a related field plus two years of related experience, or equivalent education and experience. Requires Excel, Word, electronic medical database, clinical research, data management, and coordination skills.
Microsoft Excel, Microsoft Word, electronic medical databases, Oracle, Medidata Rave, EPIC, ONCORE
DelRicht Research: Clinical research organization running embedded investigational sites and trials for patients, sponsors, and CROs across the U.S.
Early-career role; attention to detail, independent task management, clear communication, dependability, and interest in clinical research or data; training provided for systems and processes.
University of Southern California: Private research university based in Los Angeles.
0.5+ YOEExperience in clinical trials data management; data entry from medical records; regulatory compliance; sponsor coordination; data quality assurance.
University of Colorado Anschutz Medical Campus: Public academic medical campus educating health professionals, conducting medical research, and providing patient care.
1+ YOEBachelor's degree in a related field or equivalent experience; one year of clinical research experience required for intermediate level. Knowledge of clinical trials, GCP, regulations, data systems, and research protocols.
Electronic Medical Records (EMR), Electronic Health Records (EHR)
University of North Carolina at Chapel Hill: The nation's first public university conducting innovative research and teaching.
Bachelor’s degree or equivalent training and experience; strong judgment, written and verbal communication, teamwork, independence, and proficiency with Microsoft Outlook, Excel, and Word.
Microsoft Outlook, Microsoft Excel, Microsoft Word
Joint and Muscle Medical Care: Privately owned Charlotte rheumatology practice providing patient care, infusions, procedures, and clinical research trials.
2+ YOEManage clinical trials independently, ensure GCP/ICH/FDA compliance, perform participant coordination, clinical procedures, source documentation, and data management.
Clinical Data Coordinator I (CS3622 - Hamilton Wolfe)
San Antonio, Texas, United States
OnsiteFull Time
CommuniCare Health Centers: Nonprofit FQHC system providing primary, specialty, dental, behavioral, and pharmacy care to South Texas families.
1+ YOEHigh school diploma, 1+ year healthcare experience, data entry and customer service skills; EMR/EHR experience and bachelor's in life sciences preferred; bilingual English/Spanish preferred.
Yale School of Medicine: Ivy League research university in New Haven, Connecticut.
2+ YOECollect and manage clinical trial data, abstract and enter source-verified data, coordinate participant care and scheduling, use EMR and Excel, and follow HIPAA/IRB and GCP standards.
Electronic Medical Records (EMR), Microsoft Excel, Oracle, Medidata Rave, EPIC, ONCORE
Georgetown University Medical Center: Catholic academic health and science center training health professionals and scientists through research, teaching, and patient care.
2+ YOEManage and coordinate multiple clinical trials, conduct study visits, ensure protocol adherence, regulatory maintenance, timely data entry and adverse event reporting, and coordination with ancillary departments.