50 research coordinator i jobs at 4 companies in Linden, NJ
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Clinical Research Coordinator I
Bronx, New York, United States
$53k-$66k/yrOnsiteFull Time
Montefiore Medical Center: Nonprofit academic medical center providing hospital care, research and medical education for New Yorkers.
BS required; CITI and OHS certifications; experience in clinical research/clinical trials preferred; responsible for consenting, data collection, regulatory submissions, specimen handling, and coordinating multi-department trial activities.
EDCs/Databases, imaging portals, Electronic Medical Record
Columbia University Irving Medical Center: Nonprofit academic medical center providing clinical care, biomedical research, and health-professions education.
2+ YOEBachelor's degree or equivalent required; preferred candidates have 2 years of clinical research experience, strong communication and analytical skills, Microsoft Office and Excel proficiency, and familiarity with clinical research regulations and systems.
Microsoft Office, Microsoft Excel, Electronic Medical Records (EMR), Epic, REDCap, Qualtrics, iLab, OpenSpecimen, Columbia IRB
Clinical Research Coordinator I- Immunology and Immunotherapy
New York City, New York, United States
$59k-$74k/yrOnsiteFull Time
Mount Sinai Health System: Academic medical system providing comprehensive patient care and research.
0+ YOEBachelor's or master's degree in science or a related field. No experience required; research experience preferred. Requires strong organization, communication, accuracy, and patient and research-team coordination skills.
Boston or Watertown or Boston or Harlem or Bronx or Philadelphia or Dallas
$27-$32/hrOnsiteFull Time
Adams Clinical: Clinical trial site network conducting psychiatric and neurologic drug studies for pharmaceutical sponsors.
0.5+ YOEBachelor’s degree and at least 6 months of clinical research experience required; strong organization, multitasking, and willingness to develop hands-on clinical and research skills.
Columbia University: A private Ivy League research university in New York City.
Managing SHIFT trial data, maintaining IRB protocol, conducting data management and qualitative research, coordinating meetings, and liaising with team members; proficiency with REDCap and Microsoft Office required.
REDCap, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook