345 study manager jobs at 177 companies in Lodi, 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
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
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
1mo
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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
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; 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
3mo
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Clinical Research Study Manager
Jersey City, New Jersey, United States
OnsiteFull Time
5+ YOE1+ Mgmt5+ years clinical research experience; supervisory experience preferred; knowledge of FDA/ICH-GCP; training in ICH-GCP and IATA; English/Spanish bilingual preferred; Bachelor's degree preferred; ACRP certification preferred.
Electronic Data Capture (EDC), IVRS, Clinical trial management systems
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
2w
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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
3w
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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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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
1w
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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)
4w
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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
1mo
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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.
3w
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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.
2w
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Director of Study Operations
New Hyde Park or Long Island
$135k-$145k/yr RemoteFull Time
Leads clinical research operations, staff training, compliance, data management, protocol feasibility, study activation, process improvement, and site operations; master's degree and BLS/ACLS preferred.
Veeva, Clinical Trial Management System (CTMS), Electronic Health Record (EHR), Global Quality Management System (Global QMS)
4w
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Global Engagement & Study Abroad Coordinator
Riverdale, New York, United States
$61k-$68k/yr OnsiteFull Time
Bachelor's degree and prior experience with college-level study abroad or international students; attention to detail with Microsoft Excel; ability to manage budgets, travel logistics, student advising, and emergency protocols.
Microsoft Excel, SLATE, Google Drive
2w
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Executive Director, Program and Study Management, Immunology and Neurosciences
Rahway or Upper Gwynedd
$256k-$403k/yr HybridFull Time
12+ YOEBachelor's required; advanced scientific degree preferred. 12+ years clinical development experience; deep GCP/ICH knowledge, digital/AI leadership, program/study delivery and people development experience.
Artificial Intelligence (AI), eTMF
2mo
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Home Study Case Worker - Per Diem (4863)
East Orange, New Jersey, United States
$32-$35/hr FieldPart Time, Temporary
BSW or equivalent degree required, experience conducting home studies and child welfare/case management preferred, bilingual English/Spanish, strong writing and interpersonal skills, ability to travel up to 80% with limited notice.
3w
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Clinical Study Data Lead - East Hanover
East Hanover, New Jersey, United States
$120k-$222k/yr HybridFull Time
5+ YOEBachelor's in life sciences/computer science or equivalent; 5+ years clinical data management experience; strong GCP, data standards, regulatory knowledge; leadership and cross-functional influence skills.
2w
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Clinical Study Data Lead - East Hanover
East Hanover, New Jersey, United States
$120k-$222k/yr OnsiteFull Time
5+ YOEBachelor's or equivalent in life sciences/computer science,5+ years clinical data management (5–8 preferred),GCP and regulatory knowledge,leadership in cross-functional teams,data standards and analytical skills.
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