117 clinical research associate jobs at 43 companies in Waldwick, NJ
3d
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Clinical Research Associate
New York City, New York, United States
$63k-$97k/yr HybridFull Time
1+ YOERequires 1–2 years of clinical research experience, strong organization, communication, collaboration, problem-solving, and time-management skills, plus proficiency with research systems, databases, and office software.
2mo
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Clinical Research Safety Associate
Markham or Bridgewater or Shanghai or Taipei or Canada
$60k-$85k/yr HybridFull Time
2+ YOEMSc or PhD in a clinical/medical/health field, 2+ years clinical research experience in academic/pharma/CRO, Phase I-IV trial knowledge, experience with clinical data systems preferred, strong writing and MS Office skills.
Microsoft Office
2w
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Clinical Research Associate I - Center for Interventional Cardiovascular Research and Clinical Trials
New York City, New York, United States
$59k-$82k/yr OnsiteFull Time
1+ YOEBachelor's degree in life sciences or BSN and 1–2 years of relevant clinical research experience; Phase I–IV clinical study experience is highly desirable.
Clinical Trial Master File (CTMF), Clinical Trial Management (CTM), Investigator Site File (ISF), FDA
1mo
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Associate Director, Clinical Research
Paramus, New Jersey, United States
$190k-$205k/yr HybridFull Time
8+ YOE8+ years drug development/clinical research experience, Bachelor’s in science required, PMP preferred, experience with Phase II-IV trials, vendor/CRO management, regulatory compliance, strong communication and project management skills.
2w
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Clinical Research Associate I - Center for Interventional Cardiovascular Research and Clinical Trials
New York City, New York, United States
$59k-$82k/yr OnsiteFull Time
1+ YOEBachelor's degree in life sciences or BSN and 1–2 years of relevant clinical research experience; Phase I–IV study experience is highly desirable.
Microsoft Excel, Microsoft Word, Microsoft Access, Microsoft Outlook
1mo
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Clinical Research Associate (CRA) - Oncology (Remote)
Rahway or New York or Palm Springs or San Diego or Chicago or Orange County or Santa Barbara or Santa Monica or Laguna Hills or Texas or Columbia or Kansas City or St. Louis or Santa Ana or Los Angeles
$96k-$151k/yr RemoteFull Time
2+ YOERequires direct site management experience (≥2 years), clinical research knowledge (ICH/GCP), good documentation and IT skills, valid driver’s license, and ability to travel extensively.
CTMS, eTMF, MS Office
1mo
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Clinical Research Associate - Part Time
New Brunswick, New Jersey, United States
$24-$39/hr OnsitePart Time
2+ YOE2 years healthcare/research experience, proficient with Microsoft Office and CTMS, ability to recruit/consent subjects, maintain regulatory files, and manage study procedures; CCRP and phlebotomy experience preferred; Bachelor's in science/healthcare preferred.
Microsoft Office, Clinical Trial Management System (CTMS)
1w
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Senior Clinical Research Associate - Cardiovascular Medical Device
United States or New York City
$113k-$153k/yr RemoteFull Time
Bachelor’s degree in a scientific discipline and 7+ years of sponsor-side medical device clinical research experience, including study startup, site activation, enrollment, monitoring, and site management.
Good Clinical Practice (GCP), FDA medical device regulations
2w
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Clinical Research Associate, Full Service
Durham or Overland Park or Parsippany or Carlsbad
$49k-$175k/yr FieldFull Time
Bachelor's degree in science or healthcare preferred, or equivalent education and experience; clinical research regulatory knowledge, CRA training or monitoring experience, computer proficiency, English communication, and organizational skills.
Good Clinical Practice (GCP), International Conference on Harmonization (ICH), Microsoft Word, Microsoft Excel, Microsoft PowerPoint, iPhone, iPad, Trial Master File (TMF), Investigator's Site File (ISF)
1w
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Senior Clinical Research Associate, Field Monitor
United States or El Segundo or California or Los Angeles or San Diego or San Francisco or New York City or Chicago or Boston
$128k-$140k/yr RemoteFull Time
6+ YOEBachelor's degree required or RN with 5 years of on-site monitoring; 6 years of clinical trial experience, 4 years of independent monitoring, valid driver's license, and ICH-GCP knowledge required.
Risk-Based Quality Management (RBQM), Case Report Form (CRF), electronic Trial Master File (eTMF), EDC, CTMS, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook, Adobe
6d
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Clinical Research Coordinator II
Waterford or Massachusetts or Cambridge or New York City or Europe or India or Australia or North America
OnsiteFull Time
3+ YOEAssociate's or bachelor's degree in a scientific or healthcare discipline, 3–5 years of clinical research or healthcare experience, and proficiency with CTMS, EDC systems, and office software; clinical research certification preferred.
CTMS, EDC, IATA, HIPAA
2mo
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Research Associate
New York City or United States
HybridFull Time
Master's in a health-related field required; experience owning prospective clinical research (IRB protocol design, consent, enrollment), research writing, data management/QC, cross-functional collaboration, and operationalizing studies.
1mo
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Research Associate
Stamford, Connecticut, United States
$70k-$88k/yr RemoteFull Time
5+ YOEPhD in clinical psychology or related field, 5+ years research experience (including doctoral training), expertise in quantitative methods, SQL/R/Python, EHR data work, grant writing, and publication history.
SQL, R, Python, Microsoft Excel, Microsoft Word, Microsoft PowerPoint, Smartsheet
1mo
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Research Associate I
Bronx, New York, United States
$53k-$66k/yr OnsiteFull Time
Bachelor's degree and GCP training required; clinical research experience, MS Office proficiency, strong communication, attention to detail, and ability to manage multiple tasks.
Microsoft Office, Electronic Medical Record (EMR)
1mo
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FSP Sr. Clinical Research Associate II - NYC Metro or PHL - Onc
Durham or New York City or Philadelphia or New York or Pennsylvania or New Jersey or United States
$125k-$140k/yr RemoteFull Time
5+ YOE5+ years clinical monitoring experience, oncology and early-phase experience preferred; degree or allied health certification (e.g., nursing licensure); ability to perform SAE reporting and CRF review; frequent travel required.
3w
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Unblinded Clinical Research Coordinator II (4076)
Brooklyn, New York, United States
$64k-$77k/yr OnsiteFull Time
2+ YOEAssociate degree or two years of coursework and 2+ years of clinical research experience, including 1+ year as a coordinator. Requires computer proficiency and strong communication, organization, and multitasking skills.
Microsoft Word, Microsoft Excel, Microsoft Outlook, Google Suite, CRIO
1mo
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Research Associate, Pre-Clinical Vector Design
New York City, New York, United States
OnsiteFull Time
1+ YOEB.S. or M.S. in molecular biology/neuroscience, 1+ years lab experience, strong molecular biology and cell culture skills, NGS library prep, and proficiency with GraphPad Prism, FlowJo, CellProfiler, and Benchling.
GraphPad Prism, FlowJo, CellProfiler, Benchling, Next-Generation Sequencing (NGS)
4d
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Senior Clinical Trial Associate
Somerset or Bridgewater or United States
HybridFull Time
3+ YOEBachelor’s degree in life sciences, clinical research, or related field; 3–5 years as a Clinical Trial Associate or similar; oncology trial experience; knowledge of ICH-GCP and regulatory requirements; CTMS, eTMF, and EDC proficiency.
Clinical Trial Management System (CTMS), eTMF, Electronic Data Capture (EDC), Microsoft Word, Microsoft Excel, Microsoft PowerPoint
1mo
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Clinical Research Associate II / Sr. CRA (MDD Experience), Northeast US
United States or New York
$100k-$140k/yr RemoteFull Time
2+ YOEBA/BS preferred, minimum ~2 years (CRA II) or 4–5+ years (Sr CRA) onsite monitoring experience; proficiency in Microsoft Office and EDC; strong communication, organization, and critical thinking skills.
Microsoft Office, EDC
3w
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Biotech Research Associate
Arlington or New York City or San Francisco
OnsiteFull Time
1+ YOERequires 1–3 years in biotechnology or pharmaceuticals, or an advanced scientific degree; clinical data interpretation, financial modeling, advanced Excel, strong writing, and willingness to obtain FINRA licenses.
Microsoft Excel, FactSet, Bloomberg, AlphaSense, ClinicalTrials.gov, Python, R
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