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Clinical Study Manager
Fridley, Minnesota, United States
$110k-$160k/yr OnsiteFull Time
5+ YOELead clinical study execution and operations, site management, and data/regulatory compliance.
EDC systems, CTMS platforms, Clinical trial tracking tools
3w
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Clinical Study Manager
Rochester, New York, United States
$100k-$150k/yr RemoteFull Time
Bachelor's degree or equivalent, experience in clinical operations/drug-device development, ophthalmology experience preferred, knowledge of FDA/ICH/GCP/HIPAA/IRB, project management skills, strong communication and analytical abilities, Microsoft Office proficiency.
Microsoft Word, Microsoft Excel, Microsoft Outlook, Microsoft Teams, SurveyMonkey, Microsoft Forms, EDC, eCRF
1mo
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Clinical Study Manager
Plano, Texas, United States
OnsiteFull Time
3+ YOEBachelor’s in Life Sciences, Engineering, or related field; 3–8+ years clinical research; 2+ years medical device study management; ISO14155/FDA/GCP knowledge; EDC/CTMS/eTMF proficiency.
EDC, CTMS, eTMF
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
3d
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Senior Clinical Study Manager
Sunnyvale, California, United States
$152k-$218k/yr HybridFull Time
5+ YOEExperience managing multi-center premarket and post-market clinical studies, protocol/ICF development, GCP knowledge, literature review, contract/budget negotiation, team leadership, and 5+ years clinical research experience or equivalent.
Electronic Data Capture (EDC)
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
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, trial operations, vendor management, budget awareness, and strong communication and data skills.
Microsoft Project, Microsoft PowerPoint, Microsoft Word, Microsoft Excel, IVRS/IWRS, EDC, TMF
4d
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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 Project Manager
Richardson, Texas, United States
OnsiteFull Time
0.5+ YOEBachelor's preferred,6-18 months clinical research experience or equivalent,2+ years project management experience,ability to use MS Project or similar,strong communication and scheduling skills.
MS Project
3d
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Regional Clinical Study Associate Manager
United States
$96k-$131k/yr RemoteFull Time
Bachelor's degree in scientific or healthcare discipline required; experienced clinical operations professional able to manage regional study delivery, lead teams and vendors, ensure inspection readiness and compliance with ICH/GCP/SOPs.
2d
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Senior Clinical Study Manager
United States
$120k-$150k/yr RemoteFull Time
6+ YOEBachelor's in life sciences/healthcare with 8+ years or Master's with 6+ years; knowledge of GCP and regulatory requirements, IHC and IVD study experience preferred, strong communication and project management skills.
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.
1mo
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Clinical Study Operations Engineering Program Manager - Health
Sunnyvale, California, United States
OnsiteFull Time
Experience managing clinical study operations, CRO onboarding, recruitment strategy, analytics-driven insights, and international expansion for study recruitment.
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.
4d
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Senior Clinical Study Administrator
Boston, Massachusetts, United States
$83k-$124k/yr OnsiteFull Time
3+ YOEBachelor's degree in life science, ~3 years clinical operations or study support experience, proficiency with MS Office, CTMS and eTMF, strong organization, communication, and collaboration skills.
Microsoft Excel, Microsoft Word, PowerPoint, CTMS, smartsheets, eTMF
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
1mo
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Clinical Study Manager, 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 with global study oversight, CRO/vendor management, GCP/ICH compliance, risk and timeline management, and ability to travel up to 10%.
eCOA, EDC
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.
2mo
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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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Study Manager - Oncology
Morrisville, North Carolina, United States
OnsiteFull Time
Bachelor’s in life sciences or related field; CRO/pharma experience; strong GCP knowledge; excellent organizational and communication skills; travel ~25%; experience in oncology/clinical studies preferred.
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