57 clinical data associate jobs at 27 companies in Wanaque, NJ
2mo
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Associate Director, Clinical Data Management
Princeton or Madison
$171k-$207k/yr OnsiteFull Time
7+ YOE3+ MgmtBachelor’s degree in life sciences or related field; 7+ years in Biopharma/CRO with 3+ years in study leadership; strong knowledge of EDC (Medidata RAVE); travel 5-10%; leadership in data management.
Medidata RAVE, Microsoft Office
3d
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Associate Director, Clinical Data Management
Rahway or Bogotá or Munro or West Point
$142k-$224k/yr OnsiteFull Time
6+ YOEBachelor's degree, 6+ years in clinical data management or clinical research, and 3+ years using formal project management processes. Requires GCP, regulatory, leadership, mentoring, and communication skills.
3d
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Associate Director, Clinical Data Management
Rahway or Munro or Bogotá or West Point
$142k-$224k/yr OnsiteFull Time
6+ YOEBachelor's degree in life sciences, computer science, or related field; 6+ years in clinical data management or related research; 3+ years using formal project management tools and processes; leadership, regulatory, and cross-functional skills.
Good Clinical Practice (GCP)
2mo
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Associate Director, Clinical Data Management
Princeton or Madison
$171k-$207k/yr OnsiteFull Time
7+ YOE3+ MgmtBachelor's in life sciences/data science/statistics required (advanced degree preferred); 7+ years Biopharma/CRO experience with 3+ years study/program leadership; EDC/Medidata RAVE experience, Microsoft Office, FDA/ICH knowledge, project management, vendor oversight. Travel 5-10%.
EDC, Medidata RAVE, eCOA, Safety Gateway, Microsoft Office
4w
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Clinical Study Associate Manager
Armonk or Warren
$110k-$179k/yr HybridFull Time
4+ YOEBachelor's degree and 4+ years industry experience; knowledge of ICH/GCP; clinical trial operations and vendor management experience; strong communication, data-driven problem solving, and budget awareness.
Microsoft Project, Microsoft PowerPoint, Microsoft Word, Microsoft Excel, IVRS/IWRS, EDC, TMF, CTMS
1mo
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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
1mo
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Clinical Study Associate Manager
Armonk or Warren
$110k-$179k/yr OnsiteFull Time
4+ YOEBachelor's degree and 4+ years industry experience, clinical trial operations experience, knowledge of ICH/GCP, vendor management, budget awareness, strong communication and data-driven problem solving.
Microsoft Project, Microsoft PowerPoint, Microsoft Word, Microsoft Excel, IVRS/IWRS, EDC, TMF, CTMS, IVRS/IWRS
3w
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Research Data Associate, ASPIRE Trials Program
New York, New York, United States
$54k-$54k/yr OnsiteFull Time
1+ YOEAssociate's degree plus 1 year related experience (or equivalent), clinical research experience preferred, phlebotomy skills preferred, Epic EHR experience preferred, data extraction and bedside assessment skills, strong communication and organizational skills.
Epic, ELISA
1mo
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Associate Director, Clinical Science
Basking Ridge, New Jersey, United States
$162k-$244k/yr OnsiteFull Time
4+ YOEBachelor's in life sciences required; Master’s/PharmD/PhD preferred. 4+ years (PharmD/PhD) or 7+ years (Bachelor/Master) clinical experience preferred. Experience in protocol writing, study design, data review, and hematology preferred.
1mo
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Associate Director - Data Standards (Hybrid)
Florham Park or North Chicago
$142k-$269k/yr HybridFull Time
12+ YOEBSc plus 12+ years clinical research experience (10+ with MSc). Expert knowledge of CDISC standards (CDASH, SDTM, ADaM, define.xml), metadata repository governance, data mapping for regulatory submissions, and demonstrated team leadership.
CDISC, CDASH, SDTM, ADaM, define.xml, BRIDG, ODM, SHARE, eCTD, metadata repository
1mo
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Clinical Research Coordinator I
Union, New Jersey, United States
$22-$23/hr OnsiteFull Time
2+ YOEAssociate degree or 2 years relevant experience, understands clinical research and GCP, performs document review, data entry, EDC, scheduling, and study coordination.
Electronic Data Capture (EDC)
1mo
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Associate Director, Clinical Client Services
Charlotte or Denver or New York City
$160k-$190k/yr HybridFull Time
6+ YOEPharmD and active pharmacist license (or ability to obtain), 6+ years PBM/managed care experience, leadership experience, formulary/utilization/specialty pharmacy expertise, ability to translate clinical and claims data, travel up to 25%.
3d
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Clinical Coordinator
New York City, New York, United States
$64k-$68k/yr OnsiteFull Time
3+ YOE2+ MgmtRequires a bachelor's degree and 3 years' experience including 2 years supervising, or equivalent associate/high school pathways with additional experience. Requires staff leadership, data evaluation, communication, and case management software skills.
Microsoft Office Suite
1mo
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Clinical Research Assistant II - Tisch Cancer Center
New York or United States
$17-$28/hr OnsiteFull Time
2+ YOEAssociates degree or HS diploma with equivalent experience; 2 years research experience preferred. Strong communication, attention to detail, multitasking, and data entry skills for clinical study support.
Microsoft Excel, Microsoft Word, Microsoft Access, Microsoft Outlook
1mo
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Clinical Assistant-MSM-FT Days
New York, New York, United States
$27-$37/hr OnsiteFull Time
3+ YOE3 years medical assistant experience preferred; BLS from American Heart Association required; duties include patient care, EMR data entry, phlebotomy, scheduling, and mentoring junior staff.
Electronic Medical Records (EMR)
3mo
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Research Associate
Bronx, New York, United States
$56k-$70k/yr OnsiteFull Time
Supports clinical trials data collection and management under supervision; requires Bachelor's degree; prefers advanced degrees or certifications.
1mo
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Associate Dir. Cross TA Risk Management
Spring House or Horsham or Raritan or Titusville or Beerse or Basel or High Wycombe or Madrid
$122k-$213k/yr HybridFull Time
8+ YOEBachelor's in scientific/medical field, 8+ years in healthcare/pharmaceuticals or CRO/hospital, strong GCP and clinical trials experience, Health Authority inspection experience, Microsoft Office proficiency, ICH familiarity, risk management and data-analytics experience preferred, English proficiency, up to 10% travel.
Microsoft Office, Tableau, Spotfire
1mo
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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
2w
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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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