North Brunswick • 50 milesRemote · Hybrid · Onsite · Field · All Environments
North Brunswick • 50 milesRemote · Hybrid · Onsite · Field · All Environments
North Brunswick • 50 milesRemote · Hybrid · Onsite · Field · All Environments
North Brunswick • 50 milesRemote · Hybrid · Onsite · Field · All Environments
376 study manager jobs at 188 companies in North Brunswick, NJ
3mo
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Study Manager
New York City, New York, United States
OnsiteFull Time
5+ YOE5–7 years coordinating multi-site clinical studies; IRB submissions; site management; ICH-GCP; HIPAA; FDA knowledge; strong organization.
EDC, IRB platforms, eTMF, protocols, spreadsheets, data management
2mo
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Clinical Research Study Manager
Philadelphia, Pennsylvania, United States
OnsiteFull Time
5+ YOELeading clinical studies, ensuring protocol compliance, site training, data quality, and enrollment goals.
EDC, IVRS, IATA, ICH-GCP knowledge, ALCOA-C
1w
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Manager Study Start Up
Princeton, New Jersey, United States
$139k-$163k/yr OnsiteFull Time
5+ YOE5+ years experience in feasibility and study start-up, site agreements, budget negotiation, ICH/GCP knowledge, strong communication, financial acumen, and proficiency with MS Office and eTMF.
Microsoft Word, Microsoft Excel, eTMF, grant plan
1mo
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Senior Global Clinical Study Manager
Chicago or Dallas or Durham or Gilbert or Indianapolis or New York or Phoenix or Rockville or San Francisco or Tampa
$93k-$233k/yr RemoteFull Time
5+ YOE2+ MgmtBachelor's in life sciences,5+ years clinical research experience including 2+ years clinical study management; oncology and global trial experience; knowledge of ICH-GCP, regulatory requirements, financial management.
Microsoft Office, CTMS, EDC
2w
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Clinical Study Operations Manager
Boston or New York City or Paris
$90k-$110k/yr RemoteFull Time
Experience in clinical project/operations, strong project management and communication, familiarity with GCP/ICH and decentralized data collection, attention to detail, ability to manage multiple priorities.
Zendesk, Asana
3w
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Clinical Study Associate Manager
Armonk or Warren
$110k-$179k/yr HybridFull Time
4+ YOEBachelor's degree and 4+ years clinical trial experience, knowledge of ICH/GCP, vendor management, trial operations, budget awareness, and proficiency with IVRS/IWRS, EDC, TMF and MS Office.
Microsoft Project, Microsoft PowerPoint, Microsoft Word, Microsoft Excel, IVRS/IWRS, EDC, TMF
3w
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Senior Clinical Study Manager (Hybrid)
Mahwah, New Jersey, United States
$132k-$220k/yr HybridFull Time
6+ YOEBachelor's in science/healthcare, minimum 6 years clinical affairs/operations/project management in device or pharma, experience leading systems implementations, PMP/Agile/Six Sigma preferred.
clinical trial management systems, electronic data capture systems, electronic trial master files, electronic clinical outcome assessment tools, analytics, reporting, quality management systems
3w
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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; clinical trial operations, ICH/GCP knowledge, vendor management, budget awareness, and strong communication skills required.
Microsoft Project, Microsoft PowerPoint, Microsoft Word, Microsoft Excel, CTMS, TMF, IVRS/IWRS, EDC
1mo
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Senior Global Clinical Study Manager
Durham or Phoenix or Gilbert or San Francisco or New York City or Indianapolis or Tampa or Rockville or Chicago or Dallas
$93k-$233k/yr OnsiteFull Time
5+ YOE2+ MgmtBachelor's in life sciences, 5+ years clinical research/monitoring (including 2 years study management), Phase III and oncology experience, ICH-GCP and FDA knowledge, global trial and financial management, stakeholder leadership.
Microsoft Office, CTMS, EDC
1w
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Study Manager I (4078)
Philadelphia, Pennsylvania, United States
OnsiteFull Time
5+ YOEHigh school diploma required; bachelor's degree and ACRP certification preferred. Requires 5+ years of clinical research experience, strong communication, English proficiency, and clinical trial regulatory knowledge.
Electronic Data Capture (EDC), Interactive Voice Response System (IVRS)
1w
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Study Director
South Brunswick Township or Dayton
$70k-$100k/yr OnsiteFull Time
5+ YOEBachelor's degree in a related field, 5+ years overseeing biocompatibility studies, knowledge of EPA, FDA, DOT, OECD, GLP, and ISO regulations, leadership, administration, communication, and writing skills.
EPA, FDA, DOT, OECD, GLP, ISO
2w
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Study Manager I, Extractable and Leachable
Fairfield, New Jersey, United States
$65k-$90k/yr OnsiteFull Time
2+ YOEBachelor's in chemistry, 2 years E&L project experience with protocol/report writing, knowledge of HPLC/MS, GC/MS or ICP/MS, GMP familiarity, project management and strong communication skills.
HPLC/MS, GC/MS, ICP/MS, MS Office
1w
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Global Study Lead
United States or Philadelphia or Cambridge
$145k-$196k/yr HybridFull Time
7+ YOE3+ MgmtRequires a bachelor's degree, 7+ years of clinical research experience, 3–5 years leading global trials, Phase 3 experience, CRO oversight, leadership, project management, and MS Office/MS Project proficiency.
Microsoft Excel, Microsoft Word, Microsoft PowerPoint, Microsoft Project
4d
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Study Coordinator
Bronx, New York, United States
$59k/yr OnsiteFull Time
Bachelor’s degree, strong computer skills including Microsoft Excel, ability to manage multiple priorities, and teamwork required. Medical or public health research, clinical research, and Spanish proficiency preferred.
Microsoft Excel
4d
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Study Coordinator
Bronx, New York, United States
$59k/yr FieldFull Time
Bachelor's degree required; medical, public health, or clinical research preferred. Requires project coordination, strong computer skills including MS Excel, teamwork, and ability to manage multiple priorities.
Microsoft Excel, Institutional Review Board (IRB)
1w
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Global Study Lead
Cambridge or Philadelphia
$145k-$196k/yr HybridFull Time
7+ YOE3+ MgmtBachelor's degree, 7+ years of clinical research experience, and 3–5 years leading global Phase 1–4 trials including Phase 3 registrational studies. Requires CRO oversight, leadership, project management, and Microsoft Office and Project proficiency.
Microsoft Office Suite, Microsoft Excel, Microsoft Word, Microsoft PowerPoint, Microsoft Project
3w
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Associate Director, Clinical Study Management, EMEA/LATAM
Jersey City or Millbrae
$183k-$221k/yr HybridFull Time
10+ YOE10+ years related experience (or 8 with postgrad), Bachelor’s degree required, deep knowledge of ICH-GCP and regional regulations, ability to manage global oncology/neuroscience trials, budget/resource management, strong leadership and communication.
Veeva TMF
3w
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Senior Study Management Specialist
Boston or New York City
$95k-$105k/yr HybridFull Time
2+ YOEMinimum 2 years study management/clinical trial coordination experience in US clinical research; degree in a scientific discipline; strong written communication, attention to detail, and knowledge of RWE and regulatory requirements.
2w
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Manager, Independent Study Program (ISP)
New York City, New York, United States
$70k-$75k/yr OnsiteFull Time
3+ YOEBA or BFA required; MA or MFA preferred. Requires 3–5 years of related academic or museum experience, strong organization and communication, budget management, judgment, initiative, and professionalism.
1mo
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Clinical Study Manager, Global Clinical Operations (Basking Ridge, NJ, US, 07920)
Basking Ridge, New Jersey, United States
$136k-$204k/yr OnsiteFull Time
3+ YOEBSc required, 3+ years clinical trial experience, experience overseeing global trials and CRO/vendor management, knowledge of GCP/ICH, timeline/budget and risk management, study materials and site oversight; up to 10% travel.
EDC, eCOA
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