231 trial manager jobs at 87 companies in Roebling, NJ
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Clinical Trial Manager
Marlton, New Jersey, United States
$95k-$115k/yr OnsiteFull Time
4+ YOEBachelor's in scientific/clinical field, 4+ years clinical operations/clinical trial management experience (2 years for Associate level), IDE trial experience required, FDA/ICH-GCP knowledge, project management and vendor oversight skills.
Microsoft Office, clinical trial management systems
3w
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Clinical Trial Manager
Malvern, Pennsylvania, United States
OnsiteFull Time
5+ YOEBachelor’s degree in life sciences or related field; 5+ years of clinical research experience, including 2+ years as a Clinical Trial Manager; global Phase 1–3 trial and CRO oversight experience required.
Clinical Trial Management System (CTMS), Electronic Trial Master File (eTMF), Electronic Data Capture (EDC), SAS, IRT, eCOA
2mo
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Clinical Trial Manager
Princeton, New Jersey, United States
$140k-$182k/yr OnsiteFull Time
7+ YOEBA/BS and ~7 years clinical trial management experience; CRO/vendor oversight, budget and timeline management, ICH-GCP/FDA/SOP compliance, inspection readiness, Microsoft Smartsheets, 20% travel.
Microsoft Smartsheets, ICH-GCP
3w
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Senior Local Trial Manager (Sponsor Dedicated, Multiple Therapeutics)
Durham or Boston or Annapolis or Columbus or Bethlehem
$93k-$233k/yr OnsiteFull Time
3+ YOEBA/BS in a health or science field, 3–5+ years of trial management experience, complex clinical trial leadership, ICH-GCP and regulatory knowledge, strong IT skills, English and country-language proficiency, and willingness to travel.
CTMS, eTMF/IF, CAPA
1mo
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Sr. Clinical Trial Manager, Therapeutics and Oncology
Princeton, New Jersey, United States
$131k-$209k/yr OnsiteFull Time
5+ YOE5+ years clinical research experience with independent trial management, oncology/rare disease expertise, bachelor’s required (advanced preferred), strong project management, FDA/ICH GCP knowledge, and excellent communication.
1mo
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Clinical Trial Manager, Clinical Operations
Conshohocken, Pennsylvania, United States
$143k-$168k/yr OnsiteFull Time
5+ YOE5+ years clinical operations experience, knowledge of ICH-GCP and FDA regulations, experience managing global trials, strong project management and communication skills, bachelor’s in life/health sciences or equivalent.
Microsoft Office, CTMS, eTMF, EDC, IRT
2d
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Clinical Trial Supply Manager
Wavre or Zebulon or Ware or Siena or Upper Providence
€70k-€116k/yr HybridFull Time
5+ YOEUniversity degree in a relevant field and 5+ years of clinical supply, clinical operations, or clinical-trial logistics experience. Requires GxP knowledge, IRT/IVRS/IWRS experience, analytical skills, and fluent English.
IRT, IVRS, IWRS, Trial Master File (TMF), APICS, CILT, Lean Sigma, PMP, PRINCE2, Master Data Management (MDM), Materials Requirements Planning (MRP), New Product Introduction (NPI), Sales and Operations Planning (S&OP)
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Clinical Trial Liaison Manager
Bridgewater, New Jersey, United States
HybridFull Time
5+ YOEBachelor's degree required, 5+ years clinical development experience in oncology, domestic travel up to ~40%, proficiency with Microsoft Office and clinical trial systems, strong GCP/regulatory knowledge and communication skills.
Microsoft Office
4w
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Senior Trial Technician
Philadelphia, Pennsylvania, United States
OnsiteFull Time
5+ YOEBachelor's degree or equivalent, 5+ years trial technology/litigation support or video production experience, proficiency with presentation/graphics/video tools, AV troubleshooting, ability to manage multiple projects, willingness to travel 20–30% and work evenings/weekends.
2d
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Clinical Trial Manager - Investigator Initiated Studies
Philadelphia or New York or New Jersey or Pittsburgh or Atlanta or Washington or Orlando or Fairfax or Boston
$90k-$130k/yr FieldFull Time
5+ YOEBachelor's degree in science or a health-related field and 5+ years of relevant clinical research experience. Requires ICH, FDA, and European regulatory knowledge plus Microsoft Office proficiency.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint
4d
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Trial Attorney
Philadelphia, Pennsylvania, United States
OnsiteFull Time
Accredited law degree, active State Bar membership in good standing, and 3+ years of personal injury experience. Requires high-volume case management, strong writing, oral advocacy, communication, and client service skills.
3w
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Clinical Trial Supply (CTS) Study Manager
King of Prussia or Marburg or Glattbrugg
HybridFull Time
5+ YOEBachelor's degree in life sciences, engineering, logistics, or equivalent experience; 5+ years in pharmaceutical clinical supply management; ICH-GCP, cGMP, and cGDP knowledge.
interactive response technology (IRT)
2w
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Trial Attorney/Sr. Trial Attorney - Wayne, PA (Hybrid)
Wayne, Pennsylvania, United States
$130k-$189k/yr HybridFull Time
7+ YOEJuris Doctor from an ABA-accredited law school, bar membership in good standing, 7+ years of legal experience, strong legal research and writing skills, case management software proficiency, and a valid driver's license.
Microsoft Word, Microsoft Outlook, Microsoft Edge, Google Chrome, legal case management software
5d
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Clinical Trial Liaison, Director – West
Wilmington, Delaware, United States
$211k-$317k/yr FieldFull Time
3+ YOEAdvanced scientific or clinical degree; 3+ years in pharmaceutical, medical affairs, clinical development, or trial research; team leadership capability; clinical research and FDA compliance experience; 30–40% travel.
5d
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Clinical Trial Liaison, Director – East
Wilmington, Delaware, United States
$239k-$358k/yr FieldFull Time
3+ YOEAdvanced scientific or clinical degree; 3+ years in pharmaceutical, medical affairs, clinical development, or trial research; team leadership, site engagement, FDA compliance, scientific communication, and 30–40% travel required.
3w
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Senior Clinical Trial Case Manager
King of Prussia or Maidenhead
OnsiteFull Time
7+ YOEBachelor's degree or equivalent in life sciences and 7+ years of pharmacovigilance experience in multinational pharmaceuticals; requires GxP, regulatory inspection, CAPA, SOP, data, and PV process expertise.
IT
3w
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Sr. Director, TA Lead - Trial Analytics, Insights, and Planning (TAIP)
Princeton or Cambridge or Arizona or Puerto Rico or Los Angeles County
$234k-$317k/yr HybridFull Time
10+ YOE10+ years in management consulting, trial analytics, or clinical strategy; clinical trial feasibility and forecasting expertise; oncology experience; advanced degree preferred; proven global team leadership and stakeholder management.
forecasting models, dashboards, site feasibility tools
3w
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Sr. Director, TA Lead - Trial Analytics, Insights, and Planning (TAIP)
Princeton or Cambridge
$234k-$317k/yr HybridFull Time
10+ YOE10+ years in management consulting, trial analytics, or clinical strategy; clinical trial feasibility and enrollment forecasting experience; oncology expertise; team leadership; advanced degree preferred.
forecasting models, dashboards, site feasibility tools
1mo
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Clinical Trial Lead
Wayne or New Jersey or Philadelphia or United States or Parsippany or New York
$147k-$190k/yr HybridFull Time
5+ YOE2+ MgmtBachelor's in life sciences or related,5+ years clinical research experience with 2+ years leading global studies; knowledge of ICH-GCP,FDA/EMA regs; CRO/vendor and budget management; strong leadership and communication.
CTMS, eTMF, EDC
2w
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Senior Director Trial Optimization and Feasibility
West Chester, Pennsylvania, United States
$202k-$253k/yr OnsiteFull Time
12+ YOERequires 12+ years of global clinical development experience, trial optimization and feasibility leadership, complex trial expertise, CRO assumption validation, and a bachelor's degree. Neuroscience or immunology experience preferred.
DCT, Patient Surveys and Data, Tokenization, DHT, digital health
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