348 research coordinator jobs at 120 companies in Paramus, NJ
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Research Coordinator
Bronx, New York, United States
$65k-$68k/yrOnsiteFull Time
Albert Einstein College of Medicine: Academic medical school focused on education and biomedical research.
3+ YOEBachelor's degree and 3–5 years coordinating clinical research, knowledge of human subjects research, GCP, regulatory compliance, protocol interpretation, data management, and stakeholder communication.
Albert Einstein College of Medicine: Academic medical institution focused on biomedical research and education.
3+ YOEBachelor's degree in a related field,3–5 years clinical research coordination experience,knowledge of human subjects research,GCP,regulatory compliance,data management,and strong communication and project management skills.
NYU Langone Health: Academic medical system providing comprehensive patient care and education.
2+ YOEBachelor degree or equivalent; 2 years project coordination in research; proficiency in Microsoft Office; strong communication; ability to work in team and independently; willing to learn.
Microsoft Word, Microsoft Excel, Microsoft Access, Microsoft PowerPoint, Microsoft Outlook
Circuit Clinical: Operates clinical research site networks for patient-centered medical trials.
1+ YOELicensed RN or LPN required; 1+ years research coordinator or RN-level clinical experience; bachelor’s degree preferred; reliable transportation; computer literate with Microsoft Word/Excel, Google suite; CTMS experience a plus.
Microsoft Word, Microsoft Excel, Google suite, CTMS
Newark or New Brunswick or Piscataway or Scotch Plains or Blackwood or Somerset County
$71k-$101k/yrOnsiteFull Time
Rutgers University: Providing higher education degrees and conducting academic research.
2+ YOEBachelor's or Master's in a related field with 2–3+ years research experience, project management, human subjects research, MS Office, statistical software (SAS/R/SPSS), Qualtrics preferred, and ability to travel to research sites.
Catholic Health: Integrated healthcare system providing hospital and clinical medical services.
Bachelor’s in science; Master’s or MD preferred. Clinical research experience preferred. Strong organization, communication, and data management skills.
Microsoft Word, Microsoft Excel, Outlook, Electronic Data Capture (EDC) databases
Regional Cancer Care Associates: Community-based oncology and hematology healthcare and clinical research.
1+ YOECoordinate oncology clinical trials, recruit/enroll patients, maintain regulatory records, enter data into EDC/EMR/CTMS, monitor safety and protocol compliance.
Columbia University: A private Ivy League research university providing higher education.
Bachelor's degree required. Responsible for coordinating clinical research, patient recruitment and consent, data collection and regulatory maintenance. Proficient in Microsoft Office and web browsers; must complete Human Research Protection and HIPAA training. Some evening and weekend shifts; direct patient contact.
Microsoft Office, EMR, Epic, REDCap, Qualtrics, OpenSpecimen
Hackensack Meridian Health: Provides comprehensive medical care through a network of hospitals.
4+ YOEBA/BS in science or healthcare; 4+ years clinical research experience (or 2 years in senior coordinator/regulatory role); strong organization, communication, and computer skills; GCP knowledge and CCRP/CCRA/CCRC preferred.
Microsoft Office, Google Suite, clinical trial management system
Frontage LaboratoriesHKEX: 1521.HK: Provides outsourced drug discovery and development services for pharmaceutical firms.
1+ YOE1+ year clinical research experience preferred, BS/MS in biology/chemistry preferred, knowledge of GCP and FDA regulations, strong communication and organizational skills.
2+ YOEAssociate degree or 2 years relevant experience, understands clinical research and GCP, performs document review, data entry, EDC, scheduling, and study coordination.
Albert Einstein College of Medicine: Private medical school and research institution in the Bronx.
3+ YOEBachelor's degree with 3–5 years related experience (Master's preferred); IRB and protocol experience, data management, SPSS/SAS, Microsoft Office proficiency, grant and budget support.
Cushman & WakefieldNYSE: CWK: Global commercial real estate and property services firm.
0+ YOEBA/BS required, 0-1 years experience, Power BI and MS Office proficiency, strong writing, analytical and organizational skills, attention to detail, ability to work independently.
Power BI, Microsoft Excel, Microsoft Word, Microsoft PowerPoint
New York University: A private research university providing higher education degree programs.
2+ YOEBachelor's degree in a related field, 2+ years research coordination experience, applied/school-based research experience, qualitative and quantitative data collection and analysis, strong organizational and project management skills; IRB experience and Master's preferred.
Montefiore Medical Center: Academic medical center providing healthcare and clinical research services
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
Mount Sinai Health System: Integrated academic medical system providing patient care and research.
0+ YOEConduct routine human subjects research, obtain informed consent, screen participants, collect and maintain study data, and assist with regulatory and specimen handling.
Geneva Foundation: Facilitates medical research and education for the U.S. military.
2+ YOEBachelor's degree or equivalent, 2+ years clinical research or related experience preferred; knowledge of CFR, GCP, ICH, OSHA; intermediate Microsoft Excel/Office skills; organized, strong written/oral communication; government background check required.
The START Center for Cancer Research: Global network of early-phase oncology clinical trial sites.
2+ YOE2 years clinical research experience, high school diploma/GED, knowledge of oncology Phase 1 trials, GCP familiarity, strong attention to detail, organizational and communication skills, proficiency with Microsoft Office and clinical trial management software.