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Research Coordinator
Madison, Wisconsin, United States
OnsiteFull Time
Experience with large‑animal research or livestock operations, coordinating complex projects, planning/prioritizing multi‑step tasks, strong communication, and ability to follow protocols; CVT preferred; bachelor’s preferred.
1w
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Research Coordinator - In Tandem
United States
$30-$40/hr RemotePart Time, Contract
2+ YOEBachelor's degree required, 2+ years qualitative research or research operations experience, IRB/CITI experience, experience with Qualtrics, Atlas.ti, and coordinating youth listening sessions.
Atlas.ti, Qualtrics, Calendly
1w
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Clinical Research Coordinator
San Francisco, California, United States
OnsiteFull Time
Execute and coordinate clinical research protocols, interact with patients, manage data, specimens, regulatory documents, and support study operations in a hospital research setting.
Microsoft Office, Microsoft Word, Microsoft Excel, Committee of Human Research (CHR), iMEDris, Electronic Medical Records (EMR), Access, Stata, SASS, SPSS, Teleform
2mo
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Research Coordinator II
Houston, Texas, United States
OnsiteFull Time
4+ YOECoordinates day-to-day research activities, ensures data quality, and supports protocol operations. Requires bachelor’s degree and four years of research experience.
2w
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Lead Coordinator - Research
Miami Beach, Florida, United States
HybridFull Time
1+ YOE1 year medical background required; related certification and college/technical degree preferred. Role requires regulatory compliance knowledge (GCP), IRB submissions, audit support (NCI/FDA), and coordinating research operations.
1mo
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CLINICAL RESEARCH OPERATIONS COORDINATOR - FULL TIME
Maumee, Ohio, United States
OnsiteFull Time
Bachelor's required (master's preferred). Certification in Human Subjects Protection and Good Clinical Practices (GCP) within 30 days of hire. Experience in clinical research or medical practice operations, EDC/data entry, Microsoft Office, and oncology terminology.
Microsoft Office, Microsoft Word, Internet, Database, Electronic Data Capture (EDC)
1mo
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Research Operations Coordinator (CAS)
Williamsburg, Virginia, United States
$48k/yr HybridFull Time
Bachelor's degree or equivalent; administrative/financial/operational support experience; grant management familiarity; budget tracking; MS Office; strong organization and communication.
Microsoft Office, Excel, Word, Outlook
2d
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Research Coordinator II - Gastroenterology
Lebanon, New Hampshire, United States
OnsiteFull Time
2+ YOECoordinate clinical research activities for gastroenterology and obesity medicine, manage study operations, data entry, regulatory documentation, and participant communication; BLS and human subjects/GCP training required.
Clinical Trial Management System (CTMS), Electronic Data Capture (EDC)
1w
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Research Program Coordinator
Columbia, South Carolina, United States
OnsiteFull Time
Coordinate day-to-day research operations for grant-funded study on aging in women with fragile X conditions; manage participant assessments and scheduling; familiarity with REDCap; experience with clinical/human subjects research and standardized assessments preferred; strong communication, organization, and supervisory skills.
REDCap
2d
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Research Project Coordinator
Baltimore, Maryland, United States
$49k-$51k/yr OnsiteFull Time
Bachelor's degree in a scientific discipline required; prior research experience preferred. Must coordinate study operations, recruit participants, manage data, ensure regulatory compliance, and communicate with investigators.
1mo
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Research Administrative & Operations Coordinator
Minnesota, United States
$30-$31/hr HybridPart Time
2+ YOEBA/BS plus 2+ years experience (or equivalent combination totaling 6 years). Experience managing complex schedules, travel logistics, and administrative support in a research environment.
3d
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Operations Research Analyst
Scott AFB, Illinois, United States
$109k-$142k/yr OnsiteFull Time
1+ YOEBachelor's in operations research or related with 24 semester hours including calculus; 1 year specialized experience using modeling/simulation and statistical analysis in transportation/logistics; producing briefings and coordinating with stakeholders.
4d
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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
1w
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Clinical Research Coordinator
White Plains, New York, United States
$70k/yr OnsiteFull Time
Coordinate clinical trials, manage study operations and data, support IRB submissions and regulatory compliance, bachelor's degree required, clinical research certification preferred, experience with Epic, eRehab, Qualtrics, and EDC systems.
Epic, eRehab, Qualtrics, iRIS, EDC
1mo
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Sr Clinical Research Coordinator
Oklahoma City, Oklahoma, United States
$73k/yr OnsiteFull Time
4+ YOEBachelor's degree (or equivalency), 48 months clinical practice or research coordination experience, RN or PA licensure in Oklahoma, background check required, experience with clinical research operations and regulatory compliance.
3mo
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Senior Research Coordinator
United States
RemoteFull Time
5+ YOEMaster's degree in social science/research; 5+ years in operational research; design and implement performance interventions; strong writing; knowledge of DoD/IRB policies; U.S. work authorization; Tier 1 background check.
1d
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Clinical Research Coordinator
Los Angeles, California, United States
$38-$61/hr OnsiteFull Time
1+ YOECoordinate clinical trial operations, ensure regulatory compliance, prepare budgets, manage data entry and study documentation; bachelor's degree or 1-3 years coordination experience required.
2d
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CLINICAL RESEARCH COORDINATOR
Durham, North Carolina, United States
$61k-$102k/yr OnsiteFull Time
2+ YOEAssociate's degree, minimum 2 years relevant research experience, knowledge of regulatory processes, consent and safety reporting, data management, and clinical study operations.
Microsoft Office, internet browsers, OnCore, eREG, Maestro Care, iRIS, SAS, R, SPSS, NVivo, Atlas.ti, EHR, EDCs
4w
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Clinical Research Coordinator
Charleston, West Virginia, United States
OnsiteFull Time
2+ YOEManage site-level clinical trial operations, ensure regulatory compliance (GCP/SOP), coordinate patients and data entry to CTMS/EDC, maintain regulatory files, and support study documentation; 2 years site coordinating experience preferred.
FASMA Clinical Trial Management System (CTMS), EDC (Electronic Data Capture)
1mo
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Clinical Research Coordinator
Chicago, Illinois, United States
$50k-$65k/yr OnsiteFull Time
3+ YOEBachelor's or master's in social/health science (or equivalent experience), 1–3+ years research experience, mandatory NU IRB CITI training, experience managing clinical study operations, data management, and regulatory compliance (GCP/FDA/ICH).
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