310 study manager jobs at 165 companies in Bloomfield, NJ
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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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Sr. Study Manager, Clinical Operations
Princeton, New Jersey, United States
$167k-$196k/yr HybridFull Time
3+ YOELead global oncology clinical studies; manage timelines, budgets, CROs; strong leadership in Clinical Operations.
CTMS, TMF, eCRF, IRT, Central Lab, CRO management
2mo
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Sr. Study Manager, Clinical Operations
Princeton, New Jersey, United States
$167k-$196k/yr HybridFull Time
3+ YOELead global clinical studies; manage timelines and budgets; coordinate CROs/vendors; collaborate across cross-functional teams; ensure compliance.
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
4d
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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
1w
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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
2mo
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Sr. Study Manager, Clinical Operations
Princeton, New Jersey, United States
$167k-$196k/yr HybridFull Time
3+ YOE3-5 years clinical trial management; strong communication; global study leadership; familiarity with FDA/GCP/ICH; Bachelor's in biological sciences.
2w
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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
2w
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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
2w
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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
2mo
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Director, Clinical Study Management
Jersey City or Millbrae
$203k-$221k/yr HybridAll Commitments Available
12+ YOE12+ years in clinical study management; oncology focus; leadership in matrix org; strong GCP/ICh knowledge.
2mo
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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
1d
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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
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Senior Study Startup Specialist
Princeton, New Jersey, United States
$90k-$115k/yr HybridFull Time
5+ YOEBachelor's degree; 5-8 years in clinical study start-up/regulatory submissions; oncology trials; CTMS/eTMF proficiency; strong negotiation and leadership.
CTMS, eTMF, clinical trial platforms
1w
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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
2w
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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.
1w
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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
1d
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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)
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